Canonical Allele Identifier: PA2828140060
Gene: MEF2C HGNC NCBI

Linked Data

ClinVar Variation Id: 916475
ClinVar RCV Id: RCV001172160
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001351258.1:p.Met267Val
CA360423173
NM_001364329.2:c.799A>G