Allele Registry

Canonical Allele Identifier: PA110008

Gene: PHEX HGNC NCBI

ClinVar RCV:

RCV001857790

ClinVar Variation:

242795

HGVS (amino-acid)	Matching Registered Transcripts
NP_000435.3:p.Phe252Ser	CA353714 NM_000444.6:c.755T>C