Canonical Allele Identifier: PA2826259345
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1308846
ClinVar RCV Id: RCV001754734

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001189364.1:p.Tyr1031Cys
CA349060038
NM_001202435.3:c.3092A>G