Canonical Allele Identifier: PA2826841960
Gene: NPHS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1006647
ClinVar RCV Id: RCV001303724
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001284504.1:p.Glu85Lys
CA1267289
NM_001297575.2:c.253G>A