Canonical Allele Identifier: PA323551
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_056528.2:p.Thr182Ala
CA323548
NM_015713.5:c.544A>G