Canonical Allele Identifier: PA915956704
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 691837

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ala428Asp
CA389050954
NM_000257.4:c.1283C>A