Canonical Allele Identifier: PA2828140398
Gene: MEF2C HGNC NCBI

Linked Data

ClinVar Variation Id: 211492

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001351259.1:p.Ala341Thr
CA207404
NM_001364330.2:c.1021G>A