Canonical Allele Identifier: PA2826841947
Gene: NPHS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2202083
ClinVar RCV Id: RCV002629887 RCV004072102
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001284504.1:p.Ala61Thr
CA1267301
NM_001297575.2:c.181G>A