Canonical Allele Identifier: PA2826841936
Gene: NPHS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 293851
ClinVar RCV Id: RCV000297548 RCV004021379
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001284504.1:p.Arg50Trp
CA10608825
NM_001297575.2:c.148C>T