Canonical Allele Identifier: PA2828146278
Gene: MEF2C HGNC NCBI

Linked Data

ClinVar Variation Id: 211492

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001351281.1:p.Ala331Thr
CA207404
NM_001364352.2:c.991G>A