Allele Registry

Canonical Allele Identifier: PA658655052

Gene: FGF23 HGNC NCBI

ClinVar RCV:

RCV000513584

ClinVar Variation:

444062

HGVS (amino-acid)	Matching Registered Transcripts
NP_065689.1:p.Gly123Trp	CA383416436 NM_020638.3:c.367G>T