Canonical Allele Identifier: PA145076
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67706
ClinVar RCV Id: RCV000058473 RCV000156507 RCV001699115 RCV001842306 RCV004019041
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Arg680His
CA015757
NM_001099404.2:c.2039G>A