Canonical Allele Identifier: PA2825172203
Gene: PHEX HGNC NCBI

Linked Data

ClinVar Variation Id: 860072
ClinVar RCV Id: RCV001066316
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000435.3:p.Thr461Arg
CA412574722
NM_000444.6:c.1382C>G