Canonical Allele Identifier: PA2499293162
Gene: RNASEH2C HGNC NCBI

Linked Data

ClinVar Variation Id: 1056849
ClinVar RCV Id: RCV001365736 RCV002550055
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115569.2:p.Asp164Gly
CA6107595
NM_032193.4:c.491A>G