Canonical Allele Identifier: PA2828145795
Gene: MEF2C HGNC NCBI

Linked Data

ClinVar Variation Id: 211493

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001351278.1:p.His362Arg
CA208800
NM_001364349.2:c.1085A>G