Allele Registry

Canonical Allele Identifier: PA113656

Gene: RNASEH2B HGNC NCBI

ClinVar RCV:

RCV002009665

ClinVar Variation:

1508096

HGVS (amino-acid)	Matching Registered Transcripts
NP_078846.2:p.Tyr219His	CA249998464 NM_024570.4:c.655T>C