Canonical Allele Identifier: PA658654650
Gene: RNASEH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 445579
ClinVar RCV Id: RCV000514532 RCV000763423 RCV002524980
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006388.2:p.Arg186Gln
CA9231955
NM_006397.3:c.557G>A