Canonical Allele Identifier: PA916036507
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68664

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340877.1:p.Met1852Thr
CA266129
NM_001353948.2:c.5555T>C