Canonical Allele Identifier: PA658662497
Gene: PRX HGNC NCBI

Linked Data

ClinVar Variation Id: 476959
ClinVar RCV Id: RCV000550860 RCV002438494
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_870998.2:p.Gly869Arg
CA405895947
NM_181882.3:c.2605G>C
CA405895948
NM_181882.3:c.2605G>A