Canonical Allele Identifier: PA2828143559
Gene: MEF2C HGNC NCBI

Linked Data

ClinVar Variation Id: 1356476
ClinVar RCV Id: RCV001870118
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001351270.1:p.Ser263Ile
CA360423198
NM_001364341.2:c.788G>T