Canonical Allele Identifier: PA307469
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 201485
ClinVar RCV Id: RCV000183018 RCV000320680 RCV000345371 RCV000381271 RCV000265516 RCV000285751 RCV000374045 RCV001094864 RCV001842910 RCV002433810
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Arg986Trp
CA016660
NM_001099404.2:c.2956C>T