Canonical Allele Identifier: PA2826009037
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1418113

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159435.1:p.Gly271Ser
CA349073228
NM_001165963.4:c.811G>A