Canonical Allele Identifier: PA2826198754
Gene: PRODH HGNC NCBI

Linked Data

ClinVar Variation Id: 1214571

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001182155.2:p.Arg469Trp
CA10094844
NM_001195226.2:c.1405C>T