Canonical Allele Identifier: PA2826258230
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2101470
ClinVar RCV Id: RCV003016923
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001189364.1:p.Val237Leu
CA349073817
NM_001202435.3:c.709G>T
CA349073818
NM_001202435.3:c.709G>C