Canonical Allele Identifier: PA2829352775
Gene: MEF2C HGNC NCBI

Linked Data

ClinVar Variation Id: 1356476
ClinVar RCV Id: RCV001870118

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002388.2:p.Ser263Ile
CA360423198
NM_002397.5:c.788G>T