Canonical Allele Identifier: PA2826841948
Gene: NPHS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2234689
ClinVar RCV Id: RCV002731692
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001284504.1:p.Ala62Thr
CA343553199
NM_001297575.2:c.184G>A