Canonical Allele Identifier: PA2826014221
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 3158517
ClinVar RCV Id: RCV004454891

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159436.1:p.Gly1921Ser
CA349063549
NM_001165964.3:c.5761G>A