Canonical Allele Identifier: PA658807412
Gene: PRX HGNC NCBI

Linked Data

ClinVar Variation Id: 543397

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_870998.2:p.Pro1399Leu
CA9443668
NM_181882.3:c.4196C>T