Canonical Allele Identifier: PA097147
Gene: NPHP4 HGNC NCBI

Linked Data

ClinVar Variation Id: 196471
ClinVar RCV Id: RCV000177288 RCV000723456 RCV000764007 RCV001081496 RCV001097313 RCV001097312
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055917.1:p.Phe91Leu
CA243432
NM_015102.5:c.271T>C
CA338052679
NM_015102.5:c.273T>G
CA338052687
NM_015102.5:c.273T>A