Canonical Allele Identifier: PA2826066477
Gene: RRM2B HGNC NCBI

Linked Data

ClinVar Variation Id: 215094
ClinVar RCV Id: RCV000196496 RCV000714482 RCV000680084
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165949.1:p.Asn169Ser
CA320911
NM_001172478.2:c.506A>G