Canonical Allele Identifier: PA645374442
Gene: PRX HGNC NCBI

Linked Data

ClinVar Variation Id: 329275
ClinVar RCV Id: RCV000275615 RCV002521231 RCV002523067
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_870998.2:p.Leu523Pro
CA9444240
NM_181882.3:c.1568T>C