Canonical Allele Identifier: PA2828479779
Gene: NPHP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3510
ClinVar RCV Id: RCV000003685 RCV000520742 RCV000537800 RCV000778560 RCV003466797 RCV004018547
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361185.1:p.Gly286Arg
CA116310
NM_001374256.1:c.856G>A
CA348090535
NM_001374256.1:c.856G>C