Canonical Allele Identifier: PA2829676230
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2781664
ClinVar RCV Id: RCV003753385
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008851.3:p.Val1601Phe
CA349071299
NM_006920.6:c.4801G>T