Canonical Allele Identifier: PA235897
Gene: RNASEH2B HGNC NCBI

Linked Data

ClinVar Variation Id: 191042
ClinVar RCV Id: RCV000171218 RCV000492016 RCV003987401
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135751.1:p.Asp119Gly
CA235894
NM_001142279.2:c.356A>G