Canonical Allele Identifier: PA109949
Gene: PHEX HGNC NCBI

Linked Data

ClinVar Variation Id: 226119
ClinVar RCV Id: RCV000211521 RCV000396672 RCV000578203
ClinVar Variation Id: 438542
ClinVar RCV Id: RCV000505502
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000435.3:p.Gly579Arg
CA10576256
NM_000444.6:c.1735G>A
CA412575782
NM_000444.6:c.1735G>C