Canonical Allele Identifier: PA2825132624
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1748932
ClinVar RCV Id: RCV002347332
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Ser1887del
CA2580069737
NM_000335.5:c.5660_5662del