Canonical Allele Identifier: PA254801
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 9399

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Gly1262Ser
CA017513
NM_001099404.2:c.3784G>A