Canonical Allele Identifier: PA2826066522
Gene: RRM2B HGNC NCBI

Linked Data

ClinVar Variation Id: 2969690
ClinVar RCV Id: RCV003821824
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165949.1:p.Val292Ala
CA371585264
NM_001172478.2:c.875T>C