Canonical Allele Identifier: PA2827778121
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68573

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340883.1:p.Ile1910Thr
CA285030
NM_001353954.2:c.5729T>C