Canonical Allele Identifier: CA117220
Gene: FGF23 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 5028
ClinVar RCV Id: RCV000005331
dbSNP Id: rs104894343

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.4372622A>G , CM000674.2:g.4372622A>G GRCh38
NC_000012.10:g.4352049A>G NCBI36
NC_000012.11:g.4481788A>G , CM000674.1:g.4481788A>G GRCh37
NG_007087.1:g.12107T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000237837.1:c.287T>C ENSP00000237837.1:p.Met96Thr
NM_020638.2:c.287T>C VV NP_065689.1:p.Met96Thr