Canonical Allele Identifier: PA645511078
Gene: PHEX HGNC NCBI

Linked Data

ClinVar Variation Id: 438560

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000435.3:p.Glu453Asp
CA327525253
NM_000444.6:c.1359A>C
CA412574659
NM_000444.6:c.1359A>T