Canonical Allele Identifier: PA1139694309
Gene: PHEX HGNC NCBI

Linked Data

ClinVar Variation Id: 838024
ClinVar RCV Id: RCV001039487
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269683.1:p.Gly648Arg
CA412574218
NM_001282754.2:c.1942G>A
CA412574219
NM_001282754.2:c.1942G>C