Canonical Allele Identifier: PA2826842092
Gene: NPHS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 988125
ClinVar RCV Id: RCV001328094 RCV001788442
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001284504.1:p.Arg254Pro
CA1267051
NM_001297575.2:c.761G>C