Canonical Allele Identifier: PA2827761266
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 93656

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340878.1:p.Met1703Thr
CA266846
NM_001353949.2:c.5108T>C