Canonical Allele Identifier: PA2826259707
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2153965
ClinVar RCV Id: RCV003069036
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001189364.1:p.Leu1299Ser
CA1942866
NM_001202435.3:c.3896T>C