Canonical Allele Identifier: PA2828141885
Gene: MEF2C HGNC NCBI

Linked Data

ClinVar Variation Id: 424592
ClinVar RCV Id: RCV000479668

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001351264.1:p.Arg369Cys
CA16618217
NM_001364335.2:c.1105C>T