Canonical Allele Identifier: PA315918
Gene: MEF2C HGNC NCBI

Linked Data

ClinVar Variation Id: 206129

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002388.2:p.Arg15Cys
CA315916
NM_002397.5:c.43C>T