Canonical Allele Identifier: PA2826259244
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68606

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001189364.1:p.Glu954Lys
CA285102
NM_001202435.3:c.2860G>A