Canonical Allele Identifier: PA645374624
Gene: PRX HGNC NCBI

Linked Data

ClinVar Variation Id: 382637
ClinVar RCV Id: RCV000460920 RCV001173097 RCV001132595 RCV001703726
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_870998.2:p.Ala1268Pro
CA9443783
NM_181882.3:c.3802G>C