Canonical Allele Identifier: PA2580359880
Gene: NPHS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2069465
ClinVar RCV Id: RCV002962192
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055440.1:p.Ala41Gly
CA1267315
NM_014625.4:c.122C>G