Canonical Allele Identifier: PA916015543
Gene: RNASEH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 372197

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273766.1:p.Val25Ile
CA1516262
NM_001286837.3:c.73G>A