Canonical Allele Identifier: PA2826180176
Gene: MEF2C HGNC NCBI

Linked Data

ClinVar Variation Id: 538815
ClinVar RCV Id: RCV000648311

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001180278.1:p.Ala336Val
CA3337185
NM_001193349.2:c.1007C>T