Canonical Allele Identifier: PA094341
Gene: RNASEH2C HGNC NCBI

Linked Data

ClinVar Variation Id: 1260
ClinVar RCV Id: RCV000001322 RCV000414153 RCV001836687 RCV002265545
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115569.2:p.Arg69Trp
CA251720
NM_032193.4:c.205C>T