Canonical Allele Identifier: PA2499230280
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1028642
ClinVar RCV Id: RCV001329732

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ala1454Asp
CA389038921
NM_000257.4:c.4361C>A