Canonical Allele Identifier: PA2825172019
Gene: PHEX HGNC NCBI

Linked Data

ClinVar Variation Id: 2629828
ClinVar RCV Id: RCV003399901
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000435.3:p.Ile66Met
CA412567509
NM_000444.6:c.198C>G