Allele Registry

Canonical Allele Identifier: PA2499293161

Gene: RNASEH2C HGNC NCBI

ClinVar RCV:

RCV001729981

ClinVar Variation:

1299509

HGVS (amino-acid)	Matching Registered Transcripts
NP_115569.2:p.Pro138Ser	CA223999307 NM_032193.4:c.412C>T