Canonical Allele Identifier: PA2825839005
Gene: RNASEH2B HGNC NCBI

Linked Data

ClinVar Variation Id: 1410990
ClinVar RCV Id: RCV001920388
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135751.1:p.His213Gln
CA388259819
NM_001142279.2:c.639T>A
CA388259820
NM_001142279.2:c.639T>G