Canonical Allele Identifier: PA109341
Gene: RNASEH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 4641
ClinVar RCV Id: RCV000004904
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006388.2:p.Gly37Ser
CA340281
NM_006397.3:c.109G>A