Canonical Allele Identifier: PA2826092203
Gene: CRBN HGNC NCBI

Linked Data

ClinVar Variation Id: 210765

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001166953.1:p.Asp312His
CA208551
NM_001173482.1:c.934G>C