Canonical Allele Identifier: PA316567
Gene: PNPO HGNC NCBI

Linked Data

ClinVar Variation Id: 206451
ClinVar RCV Id: RCV000188499 RCV003507262
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060599.1:p.Arg225Leu
CA316566
NM_018129.4:c.674G>T