Canonical Allele Identifier: PA2826841967
Gene: NPHS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 5366
ClinVar RCV Id: RCV000005697
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001284504.1:p.Gly92Cys
CA117454
NM_001297575.2:c.274G>T