Canonical Allele Identifier: PA645403033
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 374331

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008851.3:p.Ser570Asn
CA16043652
NM_006920.6:c.1709G>A