Canonical Allele Identifier: PA2826259666
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 190028
ClinVar RCV Id: RCV000180984
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001189364.1:p.Tyr1274Ser
CA303594
NM_001202435.3:c.3821A>C