Canonical Allele Identifier: PA2499268602
Gene: NPHS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1048848
ClinVar RCV Id: RCV001354183 RCV002471093
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004637.1:p.Pro264Gln
CA9390657
NM_004646.4:c.791C>A