Canonical Allele Identifier: PA345630
Gene: RRM2B HGNC NCBI
ClinVar RCV:
RCV000119017
ClinVar Variation:
132129
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056528.2:p.Ala349Gly
CA345627
NM_015713.5:c.1046C>G