Canonical Allele Identifier: PA2827788211
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68590
ClinVar RCV Id: RCV000059466 RCV002514307 RCV003992173
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340889.1:p.Tyr761Cys
CA266101
NM_001353960.2:c.2282A>G