Allele Registry

Canonical Allele Identifier: PA099117

Gene: RRM2B HGNC NCBI

ClinVar RCV:

RCV000119012

ClinVar Variation:

132125

HGVS (amino-acid)	Matching Registered Transcripts
NP_056528.2:p.Leu317Val	CA345618 NM_015713.5:c.949T>G