Canonical Allele Identifier: PA916036436
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 189961

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340877.1:p.Arg931Pro
CA303413
NM_001353948.2:c.2792G>C