Canonical Allele Identifier: PA2826011460
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 972887

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159436.1:p.Asn115Lys
CA349076938
NM_001165964.3:c.345T>G
CA349076939
NM_001165964.3:c.345T>A