Canonical Allele Identifier: PA2825111979
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1796401

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Lys940Thr
CA389046943
NM_000257.4:c.2819A>C