Allele Registry

Canonical Allele Identifier: PA2825838763

Gene: RNASEH2B HGNC NCBI

ClinVar RCV:

RCV003062587

ClinVar Variation:

2137504

HGVS (amino-acid)	Matching Registered Transcripts
NP_001135751.1:p.Pro43His	CA249996415 NM_001142279.2:c.128C>A