Canonical Allele Identifier: PA2826014076
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68664

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159436.1:p.Met1824Thr
CA266129
NM_001165964.3:c.5471T>C