Canonical Allele Identifier: PA2826259824
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68628
ClinVar RCV Id: RCV000059506 RCV001381481 RCV001719807 RCV003989315
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001189364.1:p.Val1366Ile
CA266114
NM_001202435.3:c.4096G>A