Canonical Allele Identifier: PA2827766195
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1072727
ClinVar RCV Id: RCV001385512

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340879.1:p.Phe1278del
CA2580614386
NM_001353950.2:c.3834_3836del