Canonical Allele Identifier: PA2828146430
Gene: MEF2C HGNC NCBI

Linked Data

ClinVar Variation Id: 211492

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001351282.1:p.Ala215Thr
CA207404
NM_001364353.2:c.643G>A