Canonical Allele Identifier: PA915966141
Gene: PHEX HGNC NCBI

Linked Data

ClinVar Variation Id: 374096
ClinVar RCV Id: RCV000414906
ClinVar Variation Id: 546044
ClinVar RCV Id: RCV000657811
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000435.3:p.Phe724Ter
CA16043586
NM_000444.6:c.2167_2170dup
CA658824113
NM_000444.6:c.2171_2172del