Canonical Allele Identifier: PA2827749582
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68670
ClinVar RCV Id: RCV000059550
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340877.1:p.Asn191Tyr
CA285252
NM_001353948.2:c.571A>T