Canonical Allele Identifier: PA2826179903
Gene: MEF2C HGNC NCBI

Linked Data

ClinVar Variation Id: 538815
ClinVar RCV Id: RCV000648311

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001180277.1:p.Ala360Val
CA3337185
NM_001193348.1:c.1079C>T