Canonical Allele Identifier: PA1139693986
Gene: PHEX HGNC NCBI

Linked Data

ClinVar Variation Id: 838440
ClinVar RCV Id: RCV001039987

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269683.1:p.Gly102Arg
CA412567749
NM_001282754.2:c.304G>A
CA412567750
NM_001282754.2:c.304G>C