Canonical Allele Identifier: PA2826259904
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1705490
ClinVar RCV Id: RCV002283804

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001189364.1:p.Phe1415Cys
CA349049947
NM_001202435.3:c.4244T>G