Canonical Allele Identifier: PA208552
Gene: CRBN HGNC NCBI

Linked Data

ClinVar Variation Id: 210765

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057386.2:p.Asp313His
CA208551
NM_016302.4:c.937G>C