Allele Registry

Canonical Allele Identifier: PA099129

Gene: RRM2B HGNC NCBI

ClinVar Allele:

136345

ClinVar RCV:

RCV000119009

RCV001091699

ClinVar Variation:

132123

HGVS (amino-acid)	Matching Registered Transcripts
NP_056528.2:p.Met282Ile	CA345612 NM_015713.5:c.846G>C CA371587851 NM_015713.5:c.846G>T CA371587857 NM_015713.5:c.846G>A