Canonical Allele Identifier: PA916049361
Gene: PRODH HGNC NCBI

Linked Data

ClinVar Variation Id: 4013

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057419.5:p.Thr466Met
CA116582
NM_016335.6:c.1397C>T