Canonical Allele Identifier: PA2826842086
Gene: NPHS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 974486
ClinVar RCV Id: RCV001281253
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001284504.1:p.Ala250del
CA891813344
NM_001297575.2:c.749_751del