Canonical Allele Identifier: PA303336
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 189929
ClinVar RCV Id: RCV000180882 RCV001344647 RCV003482238
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159435.1:p.Pro768Leu
CA303333
NM_001165963.4:c.2303C>T