Allele Registry

Canonical Allele Identifier: PA106045

Gene: FGF23 HGNC NCBI

ClinVar RCV:

RCV000005331

RCV001528527

ClinVar Variation:

5028

HGVS (amino-acid)	Matching Registered Transcripts
NP_065689.1:p.Met96Thr	CA117220 NM_020638.3:c.287T>C