Canonical Allele Identifier: PA645374630
Gene: PRX HGNC NCBI

Linked Data

ClinVar Variation Id: 246123
ClinVar RCV Id: RCV000236760 RCV001094578 RCV000559953 RCV000767048 RCV001173096
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_870998.2:p.Ala1316Val
CA9443732
NM_181882.3:c.3947C>T