Allele Registry

Canonical Allele Identifier: PA106069

Gene: FGF23 HGNC NCBI

ClinVar RCV:

RCV000005332

ClinVar Variation:

5029

HGVS (amino-acid)	Matching Registered Transcripts
NP_065689.1:p.Ser129Phe	CA117221 NM_020638.3:c.386C>T