Allele Registry

Canonical Allele Identifier: PA113614

Gene: RNASEH2B HGNC NCBI

ClinVar RCV:

RCV003062587

ClinVar Variation:

2137504

HGVS (amino-acid)	Matching Registered Transcripts
NP_078846.2:p.Pro43His	CA249996415 NM_024570.4:c.128C>A