Canonical Allele Identifier: PA2826179648
Gene: MEF2C HGNC NCBI

Linked Data

ClinVar Variation Id: 538815
ClinVar RCV Id: RCV000648311

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001180276.1:p.Ala426Val
CA3337185
NM_001193347.1:c.1277C>T