Canonical Allele Identifier: PA2827787270
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68528

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340889.1:p.Arg101Gln
CA273119
NM_001353960.2:c.302G>A