Canonical Allele Identifier: PA2826397209
Gene: EPHX2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3059509
ClinVar RCV Id: RCV003974480
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243411.1:p.Lys2Arg
CA4689907
NM_001256482.2:c.5A>G