Allele Registry

Canonical Allele Identifier: PA126707

Gene: EPHX1 HGNC NCBI

ClinVar RCV:

RCV000018075

RCV000991132

RCV001610293

ClinVar Variation:

16604

HGVS (amino-acid)	Matching Registered Transcripts
NP_001129490.1:p.Tyr113His	CA126706 NM_001136018.4:c.337T>C