Canonical Allele Identifier: PA2827777902
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68569

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340883.1:p.Met1768Thr
CA285018
NM_001353954.2:c.5303T>C