Canonical Allele Identifier: PA2825537638
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 633409
ClinVar RCV Id: RCV000781838
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Ala204Thr
CA352153406
NM_001099404.2:c.610G>A