Canonical Allele Identifier: PA2827766254
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1206295
ClinVar RCV Id: RCV001573771

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340879.1:p.Glu1297Lys
CA349053289
NM_001353950.2:c.3889G>A