Allele Registry

Canonical Allele Identifier: PA094361

Gene: RNASEH2C HGNC NCBI

ClinVar RCV:

RCV000001323

ClinVar Variation:

1261

HGVS (amino-acid)	Matching Registered Transcripts
NP_115569.2:p.Lys143Ile	CA251722 NM_032193.4:c.428A>T