Canonical Allele Identifier: PA2825497566
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 68014
ClinVar RCV Id: RCV000058810 RCV000183135 RCV000208349 RCV000249083 RCV001150126 RCV001150127 RCV001150128 RCV001192713 RCV001148566 RCV001148567 RCV001148565 RCV001842396 RCV003486638
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092875.1:p.Val1933Met
CA019505
NM_001099405.2:c.5797G>A