Canonical Allele Identifier: PA2827758122
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68518

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340878.1:p.Thr801Arg
CA284895
NM_001353949.2:c.2402C>G