Allele Registry

Canonical Allele Identifier: PA109341

Gene: RNASEH2A HGNC NCBI

ClinVar RCV:

RCV000004904

ClinVar Variation:

4641

HGVS (amino-acid)	Matching Registered Transcripts
NP_006388.2:p.Gly37Ser	CA340281 NM_006397.3:c.109G>A