Canonical Allele Identifier: PA658654545
Gene: PRX HGNC NCBI

Linked Data

ClinVar Variation Id: 444468

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_870998.2:p.Pro408Ser
CA9444299
NM_181882.3:c.1222C>T