Canonical Allele Identifier: PA2825838847
Gene: RNASEH2B HGNC NCBI

Linked Data

ClinVar Variation Id: 569392
ClinVar RCV Id: RCV000690007 RCV003392525 RCV004026346
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135751.1:p.Asp105Ala
CA6985526
NM_001142279.2:c.314A>C