Canonical Allele Identifier: PA2826842094
Gene: NPHS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2734048
ClinVar RCV Id: RCV003562315
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001284504.1:p.His257Tyr
CA1267048
NM_001297575.2:c.769C>T