Canonical Allele Identifier: PA2580189607
Gene: PHEX HGNC NCBI

Linked Data

ClinVar Variation Id: 1919559
ClinVar RCV Id: RCV002594882
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269683.1:p.Ser140Leu
CA10368031
NM_001282754.2:c.419C>T