Canonical Allele Identifier: PA251731
Gene: RNASEH2B HGNC NCBI

Linked Data

ClinVar Variation Id: 1263
ClinVar RCV Id: RCV000001325 RCV001729330
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135751.1:p.Val185Gly
CA251728
NM_001142279.2:c.554T>G