Canonical Allele Identifier: PA2827765133
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 381569

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340879.1:p.Ser929Phe
CA16604035
NM_001353950.2:c.2786C>T