Canonical Allele Identifier: PA2826800184
Gene: NPHP4 HGNC NCBI

Linked Data

ClinVar Variation Id: 281976
ClinVar RCV Id: RCV000284712 RCV001087002 RCV003165723 RCV004542995
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001278522.1:p.Thr110Ala
CA554344
NM_001291593.2:c.328A>G