Canonical Allele Identifier: PA2827753677
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 189843

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340877.1:p.Pro1451Thr
CA303087
NM_001353948.2:c.4351C>A