Canonical Allele Identifier: PA2827768737
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 660951
ClinVar RCV Id: RCV000818256

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340879.1:p.His1986Arg
CA349063024
NM_001353950.2:c.5957A>G