Canonical Allele Identifier: PA2827788417
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68598

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340889.1:p.Arg902Cys
CA273369
NM_001353960.2:c.2704C>T