Canonical Allele Identifier: PA2828145519
Gene: MEF2C HGNC NCBI

Linked Data

ClinVar Variation Id: 211492

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001351277.1:p.Ala333Thr
CA207404
NM_001364348.2:c.997G>A