Allele Registry

Canonical Allele Identifier: PA113641

Gene: RNASEH2B HGNC NCBI

ClinVar RCV:

RCV000805861

ClinVar Variation:

650668

HGVS (amino-acid)	Matching Registered Transcripts
NP_078846.2:p.Thr163Ile	CA249998007 NM_024570.4:c.488C>T