Canonical Allele Identifier: PA109298
Gene: RNASEH2A HGNC NCBI
ClinVar RCV:
RCV000114338
ClinVar Variation:
126397
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006388.2:p.Arg108Trp
CA345495
NM_006397.3:c.322C>T