Allele Registry

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Canonical Allele Identifier: PA265331

Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67822

ClinVar RCV Id: RCV000058597

ClinVar Variation Id: 2691028

ClinVar RCV Id: RCV003487111

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Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000326.2:p.Val1248Asp	CA017484 NM_000335.5:c.3743T>A CA2697550807 NM_000335.5:c.3743_3744delinsAT