Canonical Allele Identifier: PA2573309883
Gene: PRX HGNC NCBI

Linked Data

ClinVar Variation Id: 1416858

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_870998.2:p.Phe799Leu
CA9444061
NM_181882.3:c.2395T>C
CA405896375
NM_181882.3:c.2397C>G
CA405896376
NM_181882.3:c.2397C>A