Canonical Allele Identifier: PA2825497155
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
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092875.1:p.Asp1801Asn
CA019238
NM_001099405.2:c.5401G>A
CA913188086
NM_001099405.2:c.5401_5403delinsAAC