Canonical Allele Identifier: PA2829403732
Gene: RNASEH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2627453
ClinVar RCV Id: RCV003388716

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002927.2:p.Leu176Phe
CA345736950
NM_002936.6:c.526C>T