Canonical Allele Identifier: PA2826731811
Gene: RNASEH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 372199
ClinVar RCV Id: RCV000412557

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273763.1:p.Ala159Val
CA16042236
NM_001286834.3:c.476C>T