Canonical Allele Identifier: PA645374440
Gene: PRX HGNC NCBI

Linked Data

ClinVar Variation Id: 246316
ClinVar RCV Id: RCV000236385 RCV000764202 RCV000802296 RCV001136189 RCV002401925 RCV003333056
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_870998.2:p.Arg516Trp
CA9444242
NM_181882.3:c.1546C>T