Canonical Allele Identifier: PA250660
Gene: EPHX2 HGNC NCBI
ClinVar RCV:
RCV000018074
ClinVar Variation:
16603
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001970.2:p.Arg287Gln
CA250659
NM_001979.6:c.860G>A