Canonical Allele Identifier: PA2826259216
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 189882
ClinVar RCV Id: RCV000180835

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001189364.1:p.Arg946Pro
CA303197
NM_001202435.3:c.2837G>C