Canonical Allele Identifier: PA2827781143
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 450573

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340884.1:p.Gln1925Glu
CA349063734
NM_001353955.2:c.5773C>G