Canonical Allele Identifier: PA658831725
Gene: NPHS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 550771
ClinVar RCV Id: RCV000665608 RCV000883029 RCV001277515
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055440.1:p.Gly42Arg
CA1267314
NM_014625.4:c.124G>A
CA343553682
NM_014625.4:c.124G>C