Canonical Allele Identifier: PA2827769578
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68581
ClinVar RCV Id: RCV000059457
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340880.1:p.Ala239Val
CA285051
NM_001353951.2:c.716C>T