Canonical Allele Identifier: PA2826260098
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1066555
ClinVar RCV Id: RCV001377575

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001189364.1:p.Pro1519Ser
CA349048587
NM_001202435.3:c.4555C>T