Canonical Allele Identifier: PA2573259548
Gene: NPHS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1555492
ClinVar RCV Id: RCV002193009
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055440.1:p.Ala59Glu
CA1267303
NM_014625.4:c.176C>A