Canonical Allele Identifier: PA2826842085
Gene: NPHS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1712399
ClinVar RCV Id: RCV002294654
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001284504.1:p.Pro248Arg
CA343565734
NM_001297575.2:c.743C>G