Canonical Allele Identifier: PA2828146709
Gene: MEF2C HGNC NCBI

Linked Data

ClinVar Variation Id: 211492

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001351283.1:p.Ala293Thr
CA207404
NM_001364354.2:c.877G>A