Canonical Allele Identifier: PA1139694206
Gene: PHEX HGNC NCBI

Linked Data

ClinVar Variation Id: 958120
ClinVar RCV Id: RCV001231229
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269683.1:p.Leu507Pro
CA412574860
NM_001282754.2:c.1520T>C