Canonical Allele Identifier: PA2827785986
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 69407
ClinVar RCV Id: RCV001304935

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340887.1:p.Lys1285Gln
CA59772659
NM_001353958.2:c.3853A>C