Canonical Allele Identifier: PA2827775830
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68502
ClinVar RCV Id: RCV000059374 RCV000180936 RCV000188861 RCV001226020 RCV001775078
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340883.1:p.Arg377Gln
CA266086
NM_001353954.2:c.1130G>A