ClinGen Allele Registry
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Canonical Allele Identifier:
PA106023
Gene: FGF23
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000029798
RCV001224010
RCV001843462
RCV002482917
ClinVar Variation:
36135
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_065689.1:p.Arg179Gln
CA213694
NM_020638.3:c.536G>A