Canonical Allele Identifier: PA2825172042
Gene: PHEX HGNC NCBI

Linked Data

ClinVar Variation Id: 1944411
ClinVar RCV Id: RCV002639753
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000435.3:p.Leu118Phe
CA10368024
NM_000444.6:c.352C>T