Canonical Allele Identifier: PA645432935
Gene: RRM2B HGNC NCBI

Linked Data

ClinVar Variation Id: 361176
ClinVar RCV Id: RCV000303281 RCV000392494 RCV003766074
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165948.1:p.Ala377Ser
CA4830963
NM_001172477.1:c.1129G>T