Canonical Allele Identifier: PA2827762199
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1483285
ClinVar RCV Id: RCV001998703

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340878.1:p.Lys1980Glu
CA1942620
NM_001353949.2:c.5938A>G