Canonical Allele Identifier: PA109912
Gene: PHEX HGNC NCBI

Linked Data

ClinVar Variation Id: 438549
ClinVar RCV Id: RCV000505475
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000435.3:p.Cys85Arg
CA412567630
NM_000444.6:c.253T>C