Canonical Allele Identifier: PA316558
Gene: PNPO HGNC NCBI

Linked Data

ClinVar Variation Id: 206446

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060599.1:p.Arg161Cys
CA316557
NM_018129.4:c.481C>T