Canonical Allele Identifier: PA2826259500
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1490559
ClinVar RCV Id: RCV002001790

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001189364.1:p.Val1169Gly
CA349056679
NM_001202435.3:c.3506T>G