Canonical Allele Identifier: PA645374506
Gene: PRX HGNC NCBI

Linked Data

ClinVar Variation Id: 410603
ClinVar RCV Id: RCV000461499 RCV000712866 RCV001136100 RCV001173750 RCV001643174 RCV002436448
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_870998.2:p.Pro850Ala
CA9444034
NM_181882.3:c.2548C>G