Canonical Allele Identifier: PA2826842004
Gene: NPHS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 5360
ClinVar RCV Id: RCV000005691 RCV000414576 RCV001003814 RCV001171338 RCV001328321 RCV001275640 RCV003944802
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001284504.1:p.Arg138Gln
CA117446
NM_001297575.2:c.413G>A