Canonical Allele Identifier: PA645468955
Gene: RNASEH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 328295
ClinVar RCV Id: RCV000967301
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006388.2:p.Ile253Thr
CA9232024
NM_006397.3:c.758T>C