Canonical Allele Identifier: PA2825839023
Gene: RNASEH2B HGNC NCBI

Linked Data

ClinVar Variation Id: 966986
ClinVar RCV Id: RCV001241791
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135751.1:p.Lys233Gln
CA6985664
NM_001142279.2:c.697A>C