Canonical Allele Identifier: PA2827776074
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 374331

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340883.1:p.Ser569Asn
CA16043652
NM_001353954.2:c.1706G>A