Canonical Allele Identifier: PA916015546
Gene: RNASEH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 372199
ClinVar RCV Id: RCV000412557
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273766.1:p.Ala68Val
CA16042236
NM_001286837.3:c.203C>T