Canonical Allele Identifier: PA2828143619
Gene: MEF2C HGNC NCBI

Linked Data

ClinVar Variation Id: 538815
ClinVar RCV Id: RCV000648311

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001351270.1:p.Ala376Val
CA3337185
NM_001364341.2:c.1127C>T