Canonical Allele Identifier: PA645374656
Gene: PRX HGNC NCBI

Linked Data

ClinVar Variation Id: 329245
ClinVar RCV Id: RCV000299891 RCV001850762 RCV002328848
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_870998.2:p.Ala1459Val
CA9443623
NM_181882.3:c.4376C>T