Allele Registry

Canonical Allele Identifier: PA109358

Gene: RNASEH2A HGNC NCBI

ClinVar RCV:

RCV000114341

ClinVar Variation:

126400

HGVS (amino-acid)	Matching Registered Transcripts
NP_006388.2:p.Thr240Met	CA345502 NM_006397.3:c.719C>T