Canonical Allele Identifier: PA658807415
Gene: PRX HGNC NCBI

Linked Data

ClinVar Variation Id: 543381
ClinVar RCV Id: RCV000654129 RCV001288694 RCV002331269
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_870998.2:p.Val1415_Ser1416insLeu
CA9443659
NM_181882.3:c.4244_4246dup