Allele Registry

Canonical Allele Identifier: PA113587

Gene: RNASEH2B HGNC NCBI

ClinVar RCV:

RCV000412805

RCV000697138

ClinVar Variation:

372780

HGVS (amino-acid)	Matching Registered Transcripts
NP_078846.2:p.Leu138Phe	CA6985560 NM_024570.4:c.412C>T