Canonical Allele Identifier: PA285248
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68668

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008851.3:p.Trp190Arg
CA285246
NM_006920.6:c.568T>C
CA349075387
NM_006920.6:c.568T>A