Canonical Allele Identifier: PA658807396
Gene: PRX HGNC NCBI

Linked Data

ClinVar Variation Id: 543486
ClinVar RCV Id: RCV000654259 RCV001811430 RCV003945683 RCV002358894
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_870998.2:p.Glu1280Gln
CA9443770
NM_181882.3:c.3838G>C