Variant "MYH7:c.1816G>T(p.Val606Leu)"
Search result: 1 record
Variant information
Gene:
Variant:
MYH7:c.1816G>T(p.Val606Leu)
HGVS:
SO Term | RefSeq |
---|---|
protein_coding | NM_000257.3:c.1816G>T(p.Val606Leu) |
dbSNP ID:
GWAS trait:
no data
Modifier statisitcs
Record:
1
Disorder:
1
Reference:
1
Effect type:
Penetrance(1)
Modifier effect:
Altered incidence(1)
Detail: