Allele Registry

Canonical Allele Identifier: PA109959

Gene: PHEX HGNC NCBI

ClinVar RCV:

RCV000412906

ClinVar Variation:

372777

HGVS (amino-acid)	Matching Registered Transcripts
NP_000435.3:p.Gly579Val	CA16043217 NM_000444.6:c.1736G>T