Canonical Allele Identifier: PA2826259589
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 976067
ClinVar RCV Id: RCV001253246
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001189364.1:p.Leu1229Pro
CA349055713
NM_001202435.3:c.3686T>C