Canonical Allele Identifier: PA2826012142
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 374331

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159436.1:p.Ser570Asn
CA16043652
NM_001165964.3:c.1709G>A