Canonical Allele Identifier: PA335874
Gene: PRX HGNC NCBI

Linked Data

ClinVar Variation Id: 216836
ClinVar RCV Id: RCV000195707 RCV000415792 RCV000493878 RCV001094576 RCV001449601 RCV001173081 RCV002426952 RCV003917822
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_870998.2:p.Leu275Ile
CA335872
NM_181882.3:c.823C>A