Canonical Allele Identifier: PA303152
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 189867
ClinVar RCV Id: RCV000180820 RCV000256008
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159435.1:p.Cys959Tyr
CA303149
NM_001165963.4:c.2876G>A