Canonical Allele Identifier: PA095065
Gene: NPHS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 5360
ClinVar RCV Id: RCV000005691 RCV000414576 RCV001003814 RCV001171338 RCV001328321 RCV001275640 RCV003944802
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055440.1:p.Arg138Gln
CA117446
NM_014625.4:c.413G>A