Canonical Allele Identifier: PA319785
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_056528.2:p.Ile159Val
CA319782
NM_015713.5:c.475A>G