Canonical Allele Identifier: PA2826259935
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2012859
ClinVar RCV Id: RCV002843428

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001189364.1:p.Thr1430Ser
CA349049638
NM_001202435.3:c.4288A>T