Allele Registry

Canonical Allele Identifier: PA094385

Gene: RNASEH2C HGNC NCBI

ClinVar RCV:

RCV000478290

RCV001851167

ClinVar Variation:

419543

HGVS (amino-acid)	Matching Registered Transcripts
NP_115569.2:p.Pro151Ser	CA6107686 NM_032193.4:c.451C>T