Canonical Allele Identifier: PA2827779874
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68530

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340884.1:p.Leu1195Pro
CA284925
NM_001353955.2:c.3584T>C