Canonical Allele Identifier: PA2580476632
Gene: RNASEH2C HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115569.2:p.Asp117His
CA381298362
NM_032193.4:c.349G>C