Canonical Allele Identifier: PA2827761542
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68657
ClinVar RCV Id: RCV000059537

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340878.1:p.Tyr1770Cys
CA285228
NM_001353949.2:c.5309A>G