Canonical Allele Identifier: PA2828140996
Gene: MEF2C HGNC NCBI

Linked Data

ClinVar Variation Id: 211493

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001351261.1:p.Thr323Ala
CA208800
NM_001364332.2:c.967A>G