Canonical Allele Identifier: PA101815
Gene: NPHP3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2633
ClinVar RCV Id: RCV000002751
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_694972.3:p.Ser360Thr
CA115652
NM_153240.5:c.1079G>C