Canonical Allele Identifier: PA110068
Gene: PHEX HGNC NCBI

Linked Data

ClinVar Variation Id: 438492
ClinVar RCV Id: RCV000505453 RCV001210936
ClinVar Variation Id: 861072
ClinVar RCV Id: RCV001067506
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000435.3:p.Trp749Arg
CA412575565
NM_000444.6:c.2245T>C
CA412575566
NM_000444.6:c.2245T>A