Canonical Allele Identifier: PA113557
Gene: RNASEH2B HGNC NCBI

Linked Data

ClinVar Variation Id: 1262
ClinVar RCV Id: RCV000001324 RCV000343151 RCV000274058 RCV001293274 RCV001813931 RCV003125824 RCV003415614 RCV004018532
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_078846.2:p.Ala177Thr
CA251724
NM_024570.4:c.529G>A