Canonical Allele Identifier: PA2825109783
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2773962
ClinVar RCV Id: RCV003532724

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ala426Thr
CA389050966
NM_000257.4:c.1276G>A