Canonical Allele Identifier: PA236808
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 191499
ClinVar RCV Id: RCV000171697 RCV000855502 RCV001842522
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Ser1738Phe
CA018989
NM_001099404.2:c.5213C>T