Allele Registry

Canonical Allele Identifier: PA109351

Gene: RNASEH2A HGNC NCBI

ClinVar RCV:

RCV000114339

ClinVar Variation:

126398

HGVS (amino-acid)	Matching Registered Transcripts
NP_006388.2:p.Phe230Leu	CA345497 NM_006397.3:c.690C>A CA404269056 NM_006397.3:c.688T>C CA404269080 NM_006397.3:c.690C>G