Canonical Allele Identifier: PA2826011542
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 418590
ClinVar RCV Id: RCV000481626
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159436.1:p.Leu170Pro
CA16617316
NM_001165964.3:c.509T>C