Canonical Allele Identifier: PA1139753608
Gene: RNASEH2B HGNC NCBI

Linked Data

ClinVar Variation Id: 952966
ClinVar RCV Id: RCV001225184
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_078846.2:p.Gly214Asp
CA249998460
NM_024570.4:c.641G>A