Canonical Allele Identifier: PA2827783559
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68556
ClinVar RCV Id: RCV000059430 RCV001339387 RCV001781396
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340886.1:p.Val1602Met
CA284988
NM_001353957.2:c.4804G>A