Canonical Allele Identifier: PA2826397298
Gene: EPHX2 HGNC NCBI
ClinVar RCV:
RCV000018074
ClinVar Variation:
16603
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243413.1:p.Arg234Gln
CA250659
NM_001256484.2:c.701G>A