Canonical Allele Identifier: PA2826842095
Gene: NPHS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2269175
ClinVar RCV Id: RCV002826160
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001284504.1:p.His257Gln
CA343565682
NM_001297575.2:c.771C>G
CA343565683
NM_001297575.2:c.771C>A