Canonical Allele Identifier: PA645374570
Gene: PRX HGNC NCBI

Linked Data

ClinVar Variation Id: 410604
ClinVar RCV Id: RCV000467624 RCV000478278 RCV001173764 RCV002451125
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_870998.2:p.Leu1194Val
CA9443829
NM_181882.3:c.3580C>G