Canonical Allele Identifier: PA645374606
Gene: PRX HGNC NCBI

Linked Data

ClinVar Variation Id: 387796
ClinVar RCV Id: RCV000546648 RCV001135977 RCV001704433
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_870998.2:p.Glu1259Lys
CA9443788
NM_181882.3:c.3775G>A