Allele Registry

Canonical Allele Identifier: PA126709

Gene: EPHX1 HGNC NCBI

ClinVar RCV:

RCV000018079

RCV001723577

ClinVar Variation:

16605

HGVS (amino-acid)	Matching Registered Transcripts
NP_001129490.1:p.His139Arg	CA126708 NM_001136018.4:c.416A>G