Canonical Allele Identifier: PA097009
Gene: NPHP4 HGNC NCBI

Linked Data

ClinVar Variation Id: 500975
ClinVar RCV Id: RCV000597836 RCV000638099 RCV000765245 RCV001096629
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055917.1:p.Ala1098Thr
CA553715
NM_015102.5:c.3292G>A