Canonical Allele Identifier: PA319786
Gene: RRM2B HGNC NCBI

Linked Data

ClinVar Variation Id: 215089
ClinVar RCV Id: RCV000195448 RCV001328923
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165948.1:p.Ile231Val
CA319782
NM_001172477.1:c.691A>G