Canonical Allele Identifier: PA2825172350
Gene: PHEX HGNC NCBI

Linked Data

ClinVar Variation Id: 1068102
ClinVar RCV Id: RCV001379551
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000435.3:p.Trp749_Ter750insLeuLeuGlyArgTrpPheMetAlaSer
CA412575578
NM_000444.6:c.2249A>T