Canonical Allele Identifier: PA2828143089
Gene: MEF2C HGNC NCBI

Linked Data

ClinVar Variation Id: 206129

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001351269.1:p.Arg15Cys
CA315916
NM_001364340.2:c.43C>T