Canonical Allele Identifier: PA2825772990
Gene: MEF2C HGNC NCBI

Linked Data

ClinVar Variation Id: 1356476
ClinVar RCV Id: RCV001870118

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001124477.1:p.Ser261Ile
CA360423198
NM_001131005.2:c.782G>T