Canonical Allele Identifier: PA2827778787
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2099693
ClinVar RCV Id: RCV003021836
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340884.1:p.Tyr362Cys
CA349071288
NM_001353955.2:c.1085A>G