Canonical Allele Identifier: PA645374519
Gene: PRX HGNC NCBI

Linked Data

ClinVar Variation Id: 245745
ClinVar RCV Id: RCV000235591 RCV001088432
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_870998.2:p.Gly1049Ser
CA9443914
NM_181882.3:c.3145G>A