Canonical Allele Identifier: PA2580462613
Gene: RNASEH2B HGNC NCBI

Linked Data

ClinVar Variation Id: 1979823
ClinVar RCV Id: RCV002756158
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_078846.2:p.Pro90Arg
CA6985520
NM_024570.4:c.269C>G