Canonical Allele Identifier: PA2826842091
Gene: NPHS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 555850
ClinVar RCV Id: RCV000671756
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001284504.1:p.Arg254Gln
CA1267052
NM_001297575.2:c.761G>A