Canonical Allele Identifier: PA2499268609
Gene: NPHS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1004356
ClinVar RCV Id: RCV001301046 RCV002493589
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004637.1:p.His842Pro
CA405392150
NM_004646.4:c.2525A>C