Allele Registry

Canonical Allele Identifier: PA2826397285

Gene: EPHX2 HGNC NCBI

ClinVar RCV:

RCV003974480

ClinVar Variation:

3059509

HGVS (amino-acid)	Matching Registered Transcripts
NP_001243413.1:p.Lys2Arg	CA4689907 NM_001256484.2:c.5A>G