Canonical Allele Identifier: PA2580476643
Gene: RNASEH2C HGNC NCBI

Linked Data

ClinVar Variation Id: 2061031
ClinVar RCV Id: RCV002942414
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115569.2:p.Pro140Gln
CA381297648
NM_032193.4:c.419C>A