Canonical Allele Identifier: PA337176
Gene: PRX HGNC NCBI

Linked Data

ClinVar Variation Id: 216834
ClinVar RCV Id: RCV000236667 RCV000416164 RCV001172781 RCV001080434 RCV001129129 RCV003947662 RCV002444813
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_870998.2:p.Glu752Lys
CA337174
NM_181882.3:c.2254G>A