Canonical Allele Identifier: PA658662584
Gene: PRX HGNC NCBI

Linked Data

ClinVar Variation Id: 476974
ClinVar Variation Id: 640692
ClinVar RCV Id: RCV000793771

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_870998.2:p.Gly1424Arg
CA9443650
NM_181882.3:c.4270G>C
CA405889935
NM_181882.3:c.4270G>A