Allele Registry

Canonical Allele Identifier: PA278598

Gene: RRM2B HGNC NCBI

ClinVar RCV:

RCV000023387

RCV000119003

ClinVar Variation:

30434

HGVS (amino-acid)	Matching Registered Transcripts
NP_056528.2:p.Phe202Leu	CA278595 NM_015713.5:c.606T>A CA371590274 NM_015713.5:c.606T>G CA371590284 NM_015713.5:c.604T>C