Canonical Allele Identifier: PA117504
Gene: RRM2B HGNC NCBI

Linked Data

ClinVar Variation Id: 5394

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165948.1:p.Arg193His
CA117501
NM_001172477.1:c.578G>A