Canonical Allele Identifier: PA285185
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68638

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008851.3:p.Val1601Ile
CA285183
NM_006920.6:c.4801G>A