Canonical Allele Identifier: PA658831735
Gene: NPHS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 555842
ClinVar RCV Id: RCV000671743 RCV001277514
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055440.1:p.Arg224His
CA1267156
NM_014625.4:c.671G>A