Canonical Allele Identifier: PA2828145487
Gene: MEF2C HGNC NCBI

Linked Data

ClinVar Variation Id: 589526
ClinVar RCV Id: RCV002316756
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001351277.1:p.Met267Thr
CA360423169
NM_001364348.2:c.800T>C