Canonical Allele Identifier: PA891855234
Gene: MEF2C HGNC NCBI

Linked Data

ClinVar Variation Id: 589526
ClinVar RCV Id: RCV002316756

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002388.2:p.Met267Thr
CA360423169
NM_002397.5:c.800T>C