Canonical Allele Identifier: PA096798
Gene: NPHS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 56471
ClinVar RCV Id: RCV000049884 RCV000793793 RCV001328089
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004637.1:p.Arg802Trp
CA250181
NM_004646.4:c.2404C>T