Canonical Allele Identifier: PA2826066480
Gene: RRM2B HGNC NCBI

Linked Data

ClinVar Variation Id: 132122
ClinVar RCV Id: RCV000119006 RCV000199478 RCV000659254 RCV002483200
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165949.1:p.Ile172Ser
CA324021
NM_001172478.2:c.515T>G