Canonical Allele Identifier: PA2827923926
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 48309
ClinVar RCV Id: RCV000041629 RCV000498301 RCV001753453 RCV004018916 RCV001841612
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341630.1:p.Arg1828His
CA019325
NM_001354701.2:c.5483G>A