Canonical Allele Identifier: PA2829675671
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2313708
ClinVar RCV Id: RCV002905094 RCV003753257
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008851.3:p.Thr1211Ile
CA349055889
NM_006920.6:c.3632C>T