Canonical Allele Identifier: PA1139747498
Gene: NPHP3 HGNC NCBI

Linked Data

ClinVar Variation Id: 951359
ClinVar RCV Id: RCV001223251 RCV002480735
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_694972.3:p.Pro1303Ser
CA2621603
NM_153240.5:c.3907C>T