Canonical Allele Identifier: PA110057
Gene: PHEX HGNC NCBI

Linked Data

ClinVar Variation Id: 438486
ClinVar RCV Id: RCV000505403
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000435.3:p.Trp530Cys
CA412575027
NM_000444.6:c.1590G>C
CA412575028
NM_000444.6:c.1590G>T