Canonical Allele Identifier: PA2826259761
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68535
ClinVar RCV Id: RCV000059408 RCV001202491 RCV003352765
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001189364.1:p.Val1335Met
CA284934
NM_001202435.3:c.4003G>A