Canonical Allele Identifier: PA2825945660
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 392829
ClinVar RCV Id: RCV000431525 RCV004000588
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153633.1:p.Asn1783Lys
CA16604559
NM_001160161.2:c.5349C>A
CA352140956
NM_001160161.2:c.5349C>G