Canonical Allele Identifier: PA913195676
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 623983
ClinVar RCV Id: RCV000762057
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008851.3:p.Ala107Val
CA349077069
NM_006920.6:c.320C>T