Canonical Allele Identifier: PA2826259557
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1308538
ClinVar RCV Id: RCV001763450
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001189364.1:p.Arg1213Gly
CA349056062
NM_001202435.3:c.3637C>G