Canonical Allele Identifier: PA2826198761
Gene: PRODH HGNC NCBI

Linked Data

ClinVar Variation Id: 2435255
ClinVar RCV Id: RCV003130339

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001182155.2:p.Phe488Leu
CA410637526
NM_001195226.2:c.1464C>G
CA410637527
NM_001195226.2:c.1464C>A
CA410637536
NM_001195226.2:c.1462T>C