Canonical Allele Identifier: PA645374449
Gene: PRX HGNC NCBI

Linked Data

ClinVar Variation Id: 242179
ClinVar RCV Id: RCV000228501 RCV000431721 RCV000658836 RCV000789549 RCV001094584 RCV002401915
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_870998.2:p.Val525Ala
CA9444239
NM_181882.3:c.1574T>C