Canonical Allele Identifier: PA2826800288
Gene: NPHP4 HGNC NCBI

Linked Data

ClinVar Variation Id: 297808

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001278522.1:p.Gly241Arg
CA554220
NM_001291593.2:c.721G>A
CA338059333
NM_001291593.2:c.721G>C