Canonical Allele Identifier: PA2826842019
Gene: NPHS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 188730
ClinVar RCV Id: RCV000169033 RCV000517983 RCV001273618 RCV001328093 RCV003407626
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001284504.1:p.Arg168His
CA199046
NM_001297575.2:c.503G>A