Canonical Allele Identifier: PA2827785020
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 374331

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340887.1:p.Ser570Asn
CA16043652
NM_001353958.2:c.1709G>A