Canonical Allele Identifier: PA2826841944
Gene: NPHS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1555492
ClinVar RCV Id: RCV002193009
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001284504.1:p.Ala59Glu
CA1267303
NM_001297575.2:c.176C>A