Canonical Allele Identifier: PA2741843371
Gene: RRM2B HGNC NCBI

Linked Data

ClinVar Variation Id: 2969690
ClinVar RCV Id: RCV003821824
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165948.1:p.Val416Ala
CA371585264
NM_001172477.1:c.1247T>C