Canonical Allele Identifier: PA2827775716
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68584
ClinVar RCV Id: RCV000059460 RCV000808399
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340883.1:p.Arg322Ile
CA285057
NM_001353954.2:c.965G>T