Allele Registry

Canonical Allele Identifier: PA1139709599

Gene: RNASEH2A HGNC NCBI

ClinVar RCV:

RCV001210471

ClinVar Variation:

940810

HGVS (amino-acid)	Matching Registered Transcripts
NP_006388.2:p.Arg291Leu	CA404270021 NM_006397.3:c.872G>T