Canonical Allele Identifier: PA645403944
Gene: RNASEH2C HGNC NCBI

Linked Data

ClinVar Variation Id: 287241
ClinVar RCV Id: RCV000385498 RCV002487247
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115569.2:p.Asp164Val
CA10605710
NM_032193.4:c.491A>T