Canonical Allele Identifier: PA207405
Gene: MEF2C HGNC NCBI

Linked Data

ClinVar Variation Id: 211492

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124477.1:p.Ala331Thr
CA207404
NM_001131005.2:c.991G>A