Canonical Allele Identifier: PA2827773608
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 189867

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340881.1:p.Cys948Tyr
CA303149
NM_001353952.2:c.2843G>A