Canonical Allele Identifier: PA2580359930
Gene: NPHS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1712399
ClinVar RCV Id: RCV002294654
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055440.1:p.Pro316Arg
CA343565734
NM_014625.4:c.947C>G