Canonical Allele Identifier: PA2828143609
Gene: MEF2C HGNC NCBI

Linked Data

ClinVar Variation Id: 424592
ClinVar RCV Id: RCV000479668

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001351270.1:p.Arg361Cys
CA16618217
NM_001364341.2:c.1081C>T