Canonical Allele Identifier: PA2827790060
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 3158517
ClinVar RCV Id: RCV004454891

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340889.1:p.Gly1920Ser
CA349063549
NM_001353960.2:c.5758G>A