Canonical Allele Identifier: PA207406
Gene: MEF2C HGNC NCBI

Linked Data

ClinVar Variation Id: 211492

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002388.2:p.Ala341Thr
CA207404
NM_002397.5:c.1021G>A