Canonical Allele Identifier: PA2826801148
Gene: NPHP4 HGNC NCBI

Linked Data

ClinVar Variation Id: 297804
ClinVar RCV Id: RCV000330012 RCV000384597 RCV000593971 RCV001093852
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001278523.1:p.Asp341Tyr
CA554063
NM_001291594.2:c.1021G>T