Canonical Allele Identifier: PA2580115275
Gene: PHEX HGNC NCBI

Linked Data

ClinVar Variation Id: 1718565
ClinVar RCV Id: RCV002299890
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000435.3:p.Asn736Ser
CA327534658
NM_000444.6:c.2207A>G