Canonical Allele Identifier: PA2826180150
Gene: MEF2C HGNC NCBI

Linked Data

ClinVar Variation Id: 211492

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001180278.1:p.Ala293Thr
CA207404
NM_001193349.2:c.877G>A