Allele Registry

Canonical Allele Identifier: PA2825838897

Gene: RNASEH2B HGNC NCBI

ClinVar RCV:

RCV000412805

RCV000697138

ClinVar Variation:

372780

HGVS (amino-acid)	Matching Registered Transcripts
NP_001135751.1:p.Leu138Phe	CA6985560 NM_001142279.2:c.412C>T