Canonical Allele Identifier: PA2826179592
Gene: MEF2C HGNC NCBI

Linked Data

ClinVar Variation Id: 1356476
ClinVar RCV Id: RCV001870118

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001180276.1:p.Ser281Ile
CA360423198
NM_001193347.1:c.842G>T