Canonical Allele Identifier: PA2827766281
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 421599
ClinVar RCV Id: RCV000483132

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340879.1:p.Lys1302Thr
CA16617296
NM_001353950.2:c.3905A>C