Canonical Allele Identifier: PA2826066452
Gene: RRM2B HGNC NCBI

Linked Data

ClinVar Variation Id: 215088
ClinVar RCV Id: RCV000199003 RCV001164963 RCV001164964 RCV002517256
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165949.1:p.Thr130Ala
CA323548
NM_001172478.2:c.388A>G