Canonical Allele Identifier: PA2826180408
Gene: MEF2C HGNC NCBI

Linked Data

ClinVar Variation Id: 1356476
ClinVar RCV Id: RCV001870118

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001180279.1:p.Ser263Ile
CA360423198
NM_001193350.2:c.788G>T