Canonical Allele Identifier: PA645374457
Gene: PRX HGNC NCBI

Linked Data

ClinVar Variation Id: 245732
ClinVar RCV Id: RCV000545891 RCV001094582 RCV001172787 RCV001705304 RCV002401919 RCV003947804
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_870998.2:p.Val551Met
CA9444221
NM_181882.3:c.1651G>A