Allele Registry

Canonical Allele Identifier: PA106038

Gene: FGF23 HGNC NCBI

ClinVar RCV:

RCV000005329

RCV000424624

ClinVar Variation:

5026

HGVS (amino-acid)	Matching Registered Transcripts
NP_065689.1:p.Arg179Trp	CA117218 NM_020638.3:c.535C>T