Canonical Allele Identifier: PA2826841950
Gene: NPHS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 555713
ClinVar RCV Id: RCV000671580
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001284504.1:p.Val65del
CA658822856
NM_001297575.2:c.194_196del