Canonical Allele Identifier: PA645455020
Gene: SCN2B HGNC NCBI

Linked Data

ClinVar Variation Id: 264461

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004579.1:p.Val160Met
CA6300424
NM_004588.5:c.478G>A