Canonical Allele Identifier: PA2826066443
Gene: RRM2B HGNC NCBI

Linked Data

ClinVar Variation Id: 361180
ClinVar RCV Id: RCV000330234 RCV000375476 RCV001850918
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165949.1:p.Lys116Arg
CA10629724
NM_001172478.2:c.347A>G