Canonical Allele Identifier: PA2827751051
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1480447
ClinVar RCV Id: RCV001985935 RCV003120792
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340877.1:p.Arg617Gly
CA349067458
NM_001353948.2:c.1849A>G