Canonical Allele Identifier: PA2825172307
Gene: PHEX HGNC NCBI

Linked Data

ClinVar Variation Id: 1452348
ClinVar RCV Id: RCV001999762
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000435.3:p.Asp646Gly
CA412574206
NM_000444.6:c.1937A>G