Canonical Allele Identifier: PA2827771037
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2637971
ClinVar RCV Id: RCV003389938
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340880.1:p.Gly1264Val
CA349054164
NM_001353951.2:c.3791G>T