Canonical Allele Identifier: PA2826918437
Gene: MEF2C HGNC NCBI

Linked Data

ClinVar Variation Id: 206129

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001294931.1:p.Arg15Cys
CA315916
NM_001308002.3:c.43C>T