Canonical Allele Identifier: PA307722
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 201521
ClinVar RCV Id: RCV000183088 RCV001144344 RCV001146240 RCV001146241 RCV001144345 RCV001146242 RCV001146243 RCV003996814
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Val1623Ile
CA018686
NM_000335.5:c.4867G>A