Canonical Allele Identifier: PA2825838799
Gene: RNASEH2B HGNC NCBI

Linked Data

ClinVar Variation Id: 1058489
ClinVar RCV Id: RCV001367637
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135751.1:p.Trp73Cys
CA388258849
NM_001142279.2:c.219G>C
CA388258850
NM_001142279.2:c.219G>T