Allele Registry

Canonical Allele Identifier: PA2825838930

Gene: RNASEH2B HGNC NCBI

ClinVar RCV:

RCV001870672

ClinVar Variation:

1369510

HGVS (amino-acid)	Matching Registered Transcripts
NP_001135751.1:p.Ser159Asn	CA388259447 NM_001142279.2:c.476G>A