Canonical Allele Identifier: PA2580476634
Gene: RNASEH2C HGNC NCBI
ClinVar RCV:
RCV003020818
ClinVar Variation:
2090252
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115569.2:p.Ala122Thr
CA381298223
NM_032193.4:c.364G>A