Allele Registry

Canonical Allele Identifier: PA109316

Gene: RNASEH2A HGNC NCBI

ClinVar RCV:

RCV000056303

RCV003155061

ClinVar Variation:

66066

HGVS (amino-acid)	Matching Registered Transcripts
NP_006388.2:p.Arg235Gln	CA345294 NM_006397.3:c.704G>A