Canonical Allele Identifier: PA2827779995
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_001340884.1:p.Tyr1262Ser
CA303594
NM_001353955.2:c.3785A>C