Canonical Allele Identifier: PA2828147236
Gene: MEF2C HGNC NCBI

Linked Data

ClinVar Variation Id: 211492

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001351286.1:p.Ala191Thr
CA207404
NM_001364357.2:c.571G>A