Canonical Allele Identifier: PA1139673609
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 924086

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Lys940Met
CA389046940
NM_000257.4:c.2819A>T