Canonical Allele Identifier: PA645374270
Gene: PRX HGNC NCBI

Linked Data

ClinVar Variation Id: 386230
ClinVar RCV Id: RCV000439721 RCV001079149 RCV001173773 RCV002328964 RCV003942403
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_870998.2:p.Ala149Thr
CA9444458
NM_181882.3:c.445G>A