Canonical Allele Identifier: PA916013935
Gene: PHEX HGNC NCBI

Linked Data

ClinVar Variation Id: 438531
ClinVar RCV Id: RCV000505436 RCV001377690
ClinVar Variation Id: 1929566
ClinVar RCV Id: RCV002618701
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269683.1:p.Lys468Asn
CA10368231
NM_001282754.2:c.1404G>C
CA412574803
NM_001282754.2:c.1404G>T