Canonical Allele Identifier: PA2580305130
Gene: SCN2B HGNC NCBI

Linked Data

ClinVar Variation Id: 1737352

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004579.1:p.Arg135His
CA6300462
NM_004588.5:c.404G>A