Canonical Allele Identifier: PA177771
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67833
ClinVar RCV Id: RCV000058610 RCV000171772 RCV000151781 RCV000417329 RCV001147537 RCV000845318 RCV001842352 RCV002354250 RCV003224134
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Phe1293Ser
CA017579
NM_001099404.2:c.3878T>C