Allele Registry

Canonical Allele Identifier: PA3057343356

Gene: RNASEH2C HGNC NCBI

ClinVar RCV:

RCV004702768

ClinVar Variation:

3339026

HGVS (amino-acid)	Matching Registered Transcripts
NP_115569.2:p.Lys143Arg	CA381297563 NM_032193.4:c.428A>G