Canonical Allele Identifier: PA916036555
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 408919

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340877.1:p.His1929Gln
CA16610265
NM_001353948.2:c.5787C>G
CA349063878
NM_001353948.2:c.5787C>A