Canonical Allele Identifier: PA251727
Gene: RNASEH2B HGNC NCBI

Linked Data

ClinVar Variation Id: 1262

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135751.1:p.Ala177Thr
CA251724
NM_001142279.2:c.529G>A