Canonical Allele Identifier: PA307350
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 201467
ClinVar RCV Id: RCV000182993 RCV000223785 RCV001842905
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Ala665Ser
CA015703
NM_001099404.2:c.1993G>T