Canonical Allele Identifier: PA265326
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67820
ClinVar RCV Id: RCV000058595 RCV000455383 RCV000618887 RCV000778920 RCV001146728 RCV001147623 RCV001146729 RCV001147622 RCV001508492 RCV001842347
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Asp1243Asn
CA017472
NM_001099404.2:c.3727G>A