Allele Registry

Canonical Allele Identifier: PA2741887038

Gene: EPHX2 HGNC NCBI

ClinVar RCV:

RCV003974480

ClinVar Variation:

3059509

HGVS (amino-acid)	Matching Registered Transcripts
NP_001970.2:p.Lys55Arg	CA4689907 NM_001979.6:c.164A>G