Canonical Allele Identifier: PA2825128512
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 532102
ClinVar RCV Id: RCV000638710 RCV000713143 RCV001146506 RCV001146501 RCV001146502 RCV001146504 RCV001841839 RCV001146503 RCV001146505 RCV002334098
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Tyr159Cys
CA063590
NM_000335.5:c.476A>G