Canonical Allele Identifier: PA2826013721
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 420883
ClinVar RCV Id: RCV000482880 RCV003221302
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159436.1:p.Thr1630Pro
CA16617285
NM_001165964.3:c.4888A>C