Canonical Allele Identifier: PA2827789430
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68552

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340889.1:p.Cys1559Arg
CA284979
NM_001353960.2:c.4675T>C