Canonical Allele Identifier: PA658682248
Gene: NPHS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 450011
ClinVar RCV Id: RCV000519536 RCV001829486
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004637.1:p.Ser536Pro
CA405400147
NM_004646.4:c.1606T>C