Canonical Allele Identifier: PA2580380899
Gene: RRM2B HGNC NCBI

Linked Data

ClinVar Variation Id: 2435485
ClinVar RCV Id: RCV003135807
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056528.2:p.Ala61Pro
CA371595883
NM_015713.5:c.181G>C