Canonical Allele Identifier: PA916044863
Gene: MEF2C HGNC NCBI

Linked Data

ClinVar Variation Id: 211492

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001351267.1:p.Ala351Thr
CA207404
NM_001364338.2:c.1051G>A