Canonical Allele Identifier: PA658829063
Gene: NPHS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 550087
ClinVar RCV Id: RCV000664718 RCV001731855 RCV002532034
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004637.1:p.Ser572Gly
CA9390359
NM_004646.4:c.1714A>G