Canonical Allele Identifier: PA2827756530
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1418113

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340878.1:p.Gly271Ser
CA349073228
NM_001353949.2:c.811G>A