Allele Registry

Canonical Allele Identifier: PA106009

Gene: FGF23 HGNC NCBI

ClinVar RCV:

RCV000005328

RCV000254829

ClinVar Variation:

5025

HGVS (amino-acid)	Matching Registered Transcripts
NP_065689.1:p.Arg176Gln	CA117217 NM_020638.3:c.527G>A