Allele Registry

Canonical Allele Identifier: PA2826066502

Gene: RRM2B HGNC NCBI

ClinVar Allele:

136345

ClinVar RCV:

RCV000119009

RCV001091699

ClinVar Variation:

132123

HGVS (amino-acid)	Matching Registered Transcripts
NP_001165949.1:p.Met230Ile	CA345612 NM_001172478.2:c.690G>C CA371587851 NM_001172478.2:c.690G>T CA371587857 NM_001172478.2:c.690G>A