Canonical Allele Identifier: PA303415
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 189961

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008851.3:p.Arg920Pro
CA303413
NM_006920.6:c.2759G>C