Canonical Allele Identifier: PA645374483
Gene: PRX HGNC NCBI

Linked Data

ClinVar Variation Id: 329271
ClinVar RCV Id: RCV001173084 RCV001706526 RCV000544205 RCV001094571 RCV002487453
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_870998.2:p.Pro655Leu
CA9444159
NM_181882.3:c.1964C>T