Canonical Allele Identifier: PA2827773431
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 93639

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340881.1:p.Arg848His
CA266833
NM_001353952.2:c.2543G>A