Canonical Allele Identifier: PA303266
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 189904
ClinVar RCV Id: RCV000180856
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008851.3:p.Gly177Val
CA303263
NM_006920.6:c.530G>T