Canonical Allele Identifier: PA174146
Gene: KPRP HGNC NCBI

Linked Data

ClinVar Variation Id: 161498
ClinVar RCV Id: RCV000149032

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001020402.1:p.Phe275Leu
CA174145
NM_001025231.3:c.825T>A
CA342501670
NM_001025231.3:c.823T>C
CA342501675
NM_001025231.3:c.825T>G