Canonical Allele Identifier: PA265373
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67838
ClinVar RCV Id: RCV000058616 RCV000252945 RCV000505769 RCV000709762 RCV001553760 RCV001842356 RCV002483113
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Gly1319Val
CA017654
NM_001099404.2:c.3956G>T