Allele Registry

Canonical Allele Identifier: PA106075

Gene: FGF23 HGNC NCBI

ClinVar RCV:

RCV000005330

RCV000412723

RCV000662354

RCV000984806

ClinVar Variation:

5027

HGVS (amino-acid)	Matching Registered Transcripts
NP_065689.1:p.Ser71Gly	CA117219 NM_020638.3:c.211A>G