Canonical Allele Identifier: PA645502452
Gene: NPHP4 HGNC NCBI

Linked Data

ClinVar Variation Id: 289039

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055917.1:p.Arg88Lys
CA10606304
NM_015102.5:c.263G>A