Canonical Allele Identifier: PA335928
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 216841
ClinVar RCV Id: RCV000498992 RCV001842951 RCV003539815
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Tyr1950Cys
CA335923
NM_001099404.2:c.5849A>G