Canonical Allele Identifier: PA645495468
Gene: RNASEH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 372199
ClinVar RCV Id: RCV000412557
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002927.2:p.Ala185Val
CA16042236
NM_002936.6:c.554C>T