Allele Registry

Canonical Allele Identifier: PA2573284099

Gene: RNASEH2B HGNC NCBI

ClinVar Allele:

1414522

ClinVar RCV:

RCV001870672

ClinVar Variation:

1369510

HGVS (amino-acid)	Matching Registered Transcripts
NP_078846.2:p.Ser159Asn	CA388259447 NM_024570.4:c.476G>A