Canonical Allele Identifier: PA278608
Gene: RRM2B HGNC NCBI

Linked Data

ClinVar Variation Id: 30436
ClinVar RCV Id: RCV000023389 RCV000118993 RCV001852021 RCV002283445
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165948.1:p.Pro105Ser
CA278605
NM_001172477.1:c.313C>T