Canonical Allele Identifier: PA2826918682
Gene: MEF2C HGNC NCBI

Linked Data

ClinVar Variation Id: 538815
ClinVar RCV Id: RCV000648311

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001294931.1:p.Ala408Val
CA3337185
NM_001308002.3:c.1223C>T