Canonical Allele Identifier: PA2828147092
Gene: MEF2C HGNC NCBI

Linked Data

ClinVar Variation Id: 538815
ClinVar RCV Id: RCV000648311

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001351285.1:p.Ala258Val
CA3337185
NM_001364356.2:c.773C>T