Canonical Allele Identifier: PA107846
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 9399
ClinVar RCV Id: RCV000010001 RCV000058602 RCV000755698 RCV001146725 RCV001146726 RCV001146727 RCV001753410 RCV003996086 RCV004018613 RCV004528100
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Gly1262Ser
CA017513
NM_198056.3:c.3784G>A