Canonical Allele Identifier: PA2741915331
Gene: SCN2B HGNC NCBI

Linked Data

ClinVar Variation Id: 2713121
ClinVar RCV Id: RCV003582467
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004579.1:p.Gly168Cys
CA6300419
NM_004588.5:c.502G>T