Canonical Allele Identifier: PA2828145020
Gene: MEF2C HGNC NCBI

Linked Data

ClinVar Variation Id: 211493

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001351275.1:p.His370Arg
CA208800
NM_001364346.2:c.1109A>G