Canonical Allele Identifier: PA645374491
Gene: PRX HGNC NCBI

Linked Data

ClinVar Variation Id: 388340
ClinVar RCV Id: RCV000811458 RCV001704468 RCV002522436 RCV003970203
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_870998.2:p.Met722Val
CA9444114
NM_181882.3:c.2164A>G