Canonical Allele Identifier: PA204017
Gene: RRM2B HGNC NCBI

Linked Data

ClinVar Variation Id: 132109
ClinVar RCV Id: RCV000005720 RCV000118988 RCV000186558 RCV000413797 RCV002483199
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165948.1:p.Glu157del
CA204014
NM_001172477.1:c.469_471del