Canonical Allele Identifier: PA2827765987
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68618
ClinVar RCV Id: RCV000059495
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340879.1:p.Ser1220Thr
CA285132
NM_001353950.2:c.3659G>C