Canonical Allele Identifier: PA2825112171
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2773936

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ala1051Thr
CA389045369
NM_000257.4:c.3151G>A