Canonical Allele Identifier: PA2825839011
Gene: RNASEH2B HGNC NCBI

Linked Data

ClinVar Variation Id: 452949
ClinVar RCV Id: RCV000519718
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135751.1:p.Ser217Pro
CA249998463
NM_001142279.2:c.649T>C