Canonical Allele Identifier: PA645375434
Gene: NPHS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 328870
ClinVar RCV Id: RCV000271950
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004637.1:p.Leu533Pro
CA10652376
NM_004646.4:c.1598T>C