Allele Registry

Canonical Allele Identifier: PA278962

Gene: FGF23 HGNC NCBI

ClinVar RCV:

RCV000197637

ClinVar Variation:

216929

HGVS (amino-acid)	Matching Registered Transcripts
NP_065689.1:p.Gly87Asp	CA278961 NM_020638.3:c.260G>A