Canonical Allele Identifier: PA345631
Gene: RRM2B HGNC NCBI
ClinVar RCV:
RCV000119017
ClinVar Variation:
132129
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165948.1:p.Ala421Gly
CA345627
NM_001172477.1:c.1262C>G