Canonical Allele Identifier: PA1139753605
Gene: RNASEH2B HGNC NCBI

Linked Data

ClinVar Variation Id: 871584
ClinVar RCV Id: RCV001091632
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_078846.2:p.Ala212Thr
CA388259808
NM_024570.4:c.634G>A