Canonical Allele Identifier: PA096752
Gene: NPHS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 56438
ClinVar RCV Id: RCV000049851 RCV001388275 RCV001849302 RCV002294008
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004637.1:p.Arg460Gln
CA250119
NM_004646.4:c.1379G>A