Canonical Allele Identifier: PA2826259550
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1065175
ClinVar RCV Id: RCV001375623
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001189364.1:p.Arg1209Trp
CA349056089
NM_001202435.3:c.3625A>T