Canonical Allele Identifier: PA2825839000
Gene: RNASEH2B HGNC NCBI

Linked Data

ClinVar Variation Id: 1427436
ClinVar RCV Id: RCV001933709
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135751.1:p.Tyr211His
CA388259803
NM_001142279.2:c.631T>C