Canonical Allele Identifier: PA2826066525
Gene: RRM2B HGNC NCBI
ClinVar RCV:
RCV000119017
ClinVar Variation:
132129
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165949.1:p.Ala297Gly
CA345627
NM_001172478.2:c.890C>G