Canonical Allele Identifier: PA2825945047
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 418616
ClinVar RCV Id: RCV000481094
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153633.1:p.Tyr1393His
CA16617946
NM_001160161.2:c.4177T>C