Canonical Allele Identifier: PA2829846956
Gene: RRM2B HGNC NCBI

Linked Data

ClinVar Variation Id: 2683026
ClinVar RCV Id: RCV003481893

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056528.2:p.Pro118Ser
CA371593161
NM_015713.5:c.352C>T