Canonical Allele Identifier: PA2573284120
Gene: RNASEH2B HGNC NCBI

Linked Data

ClinVar Variation Id: 1410053
ClinVar RCV Id: RCV001916247
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_078846.2:p.Tyr208Cys
CA388259786
NM_024570.4:c.623A>G