Allele Registry

Canonical Allele Identifier: PA113675

Gene: RNASEH2B HGNC NCBI

ClinVar RCV:

RCV000001325

RCV001729330

ClinVar Variation:

1263

HGVS (amino-acid)	Matching Registered Transcripts
NP_078846.2:p.Val185Gly	CA251728 NM_024570.4:c.554T>G