Canonical Allele Identifier: PA2827789822
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 68660

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340889.1:p.Glu1766Lys
CA266126
NM_001353960.2:c.5296G>A