Canonical Allele Identifier: PA2580157447
Gene: RRM2B HGNC NCBI

Linked Data

ClinVar Variation Id: 1927163
ClinVar RCV Id: RCV002631033
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165948.1:p.Glu266Gln
CA4831048
NM_001172477.1:c.796G>C