Canonical Allele Identifier: PA2826260463
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 834858
ClinVar RCV Id: RCV001035628

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001189364.1:p.Asp1727Tyr
CA349068756
NM_001202435.3:c.5179G>T