Allele Registry

Canonical Allele Identifier: PA113598

Gene: RNASEH2B HGNC NCBI

ClinVar RCV:

RCV000794275

ClinVar Variation:

641111

HGVS (amino-acid)	Matching Registered Transcripts
NP_078846.2:p.Leu60Arg	CA249996620 NM_024570.4:c.179T>G