Canonical Allele Identifier: PA2826397262
Gene: EPHX2 HGNC NCBI
ClinVar RCV:
RCV000018074
ClinVar Variation:
16603
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243412.1:p.Arg221Gln
CA250659
NM_001256483.2:c.662G>A