Canonical Allele Identifier: PA2825112276
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2773928
ClinVar RCV Id: RCV003532691

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Arg1126His
CA257815799
NM_000257.4:c.3377G>A