Allele Registry

Canonical Allele Identifier: PA094395

Gene: RNASEH2C HGNC NCBI

ClinVar RCV:

RCV000994660

RCV001823174

ClinVar Variation:

806694

HGVS (amino-acid)	Matching Registered Transcripts
NP_115569.2:p.Pro76Leu	CA6107764 NM_032193.4:c.227C>T