Canonical Allele Identifier: PA658807422
Gene: PRX HGNC NCBI

Linked Data

ClinVar Variation Id: 543355
ClinVar RCV Id: RCV000654099 RCV000757696 RCV001131558 RCV001173755 RCV002331268 RCV003147528
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_870998.2:p.Arg1436Gln
CA9443644
NM_181882.3:c.4307G>A