Canonical Allele Identifier: PA2826842116
Gene: NPHS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1344835
ClinVar RCV Id: RCV001849837
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001284504.1:p.Asn306Tyr
CA343565208
NM_001297575.2:c.916A>T