Canonical Allele Identifier: PA120374
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 9402
ClinVar RCV Id: RCV000010005 RCV000058782 RCV000171695 RCV000183199 RCV000987198 RCV001507624 RCV002345238 RCV001841243
ClinVar Variation Id: 920535
ClinVar RCV Id: RCV001842769 RCV002491518 RCV003163406
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Asp1819Asn
CA019238
NM_001099404.2:c.5455G>A
CA913188086
NM_001099404.2:c.5455_5457delinsAAC