Allele Registry

Canonical Allele Identifier: PA345615

Gene: RRM2B HGNC NCBI

ClinVar Allele:

136345

ClinVar RCV:

RCV000119009

RCV001091699

ClinVar Variation:

132123

HGVS (amino-acid)	Matching Registered Transcripts
NP_001165948.1:p.Met354Ile	CA345612 NM_001172477.1:c.1062G>C CA371587851 NM_001172477.1:c.1062G>T CA371587857 NM_001172477.1:c.1062G>A