Canonical Allele Identifier: PA916036460
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68606

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340877.1:p.Glu954Lys
CA285102
NM_001353948.2:c.2860G>A