Canonical Allele Identifier: PA2827788472
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68606

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340889.1:p.Glu925Lys
CA285102
NM_001353960.2:c.2773G>A