Canonical Allele Identifier: PA2825172038
Gene: PHEX HGNC NCBI

Linked Data

ClinVar Variation Id: 1519035
ClinVar RCV Id: RCV002024302
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000435.3:p.Gly102Trp
CA412567751
NM_000444.6:c.304G>T