Canonical Allele Identifier: PA2825944686
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 3074195
ClinVar RCV Id: RCV004012737
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153633.1:p.Leu1162Pro
CA352138007
NM_001160161.2:c.3485T>C