Canonical Allele Identifier: PA109306
Gene: RNASEH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 66068
ClinVar RCV Id: RCV000056305 RCV000610608 RCV003894911
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006388.2:p.Arg186Trp
CA345300
NM_006397.3:c.556C>T