Canonical Allele Identifier: PA645374537
Gene: PRX HGNC NCBI

Linked Data

ClinVar Variation Id: 245663
ClinVar RCV Id: RCV000235608 RCV001172782 RCV000658835 RCV001085498 RCV001128999 RCV001358805 RCV002450720
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_870998.2:p.Gly1125Ser
CA9443872
NM_181882.3:c.3373G>A