Canonical Allele Identifier: PA2828146392
Gene: MEF2C HGNC NCBI

Linked Data

ClinVar Variation Id: 1356476
ClinVar RCV Id: RCV001870118

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001351282.1:p.Ser137Ile
CA360423198
NM_001364353.2:c.410G>T