Canonical Allele Identifier: PA2580528451
Gene: NPHP3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2330639
ClinVar RCV Id: RCV002935010

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_694972.3:p.Met565Leu
CA354583014
NM_153240.5:c.1693A>T
CA354583015
NM_153240.5:c.1693A>C