Canonical Allele Identifier: PA108623
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68509
ClinVar RCV Id: RCV000059381
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159435.1:p.Tyr413Asn
CA284877
NM_001165963.4:c.1237T>A