Canonical Allele Identifier: PA285080
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68596

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008851.3:p.Phe90Ser
CA285078
NM_006920.6:c.269T>C