Canonical Allele Identifier: PA2827774797
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68565

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340881.1:p.Cys1705Arg
CA285006
NM_001353952.2:c.5113T>C