Canonical Allele Identifier: PA2827761795
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68664

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340878.1:p.Met1841Thr
CA266129
NM_001353949.2:c.5522T>C