Canonical Allele Identifier: PA2573291532
Gene: RNASEH2C HGNC NCBI

Linked Data

ClinVar Variation Id: 1392250
ClinVar RCV Id: RCV001896124
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115569.2:p.Ala147Val
CA381297442
NM_032193.4:c.440C>T