Canonical Allele Identifier: PA2580408924
Gene: PRODH HGNC NCBI

Linked Data

ClinVar Variation Id: 2435255
ClinVar RCV Id: RCV003130339

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057419.5:p.Phe596Leu
CA410637526
NM_016335.6:c.1788C>G
CA410637527
NM_016335.6:c.1788C>A
CA410637536
NM_016335.6:c.1786T>C