Canonical Allele Identifier: PA2826842097
Gene: NPHS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1303204
ClinVar RCV Id: RCV001756703 RCV003346665
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001284504.1:p.Gln260Arg
CA343565666
NM_001297575.2:c.779A>G