Canonical Allele Identifier: PA2573240035
Gene: NPHS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1520417
ClinVar RCV Id: RCV002024973 RCV003289403
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004637.1:p.Ala325Ser
CA9390590
NM_004646.4:c.973G>T