Canonical Allele Identifier: PA2580335075
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1801821

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008851.3:p.Thr105Asn
CA59804349
NM_006920.6:c.314C>A