Canonical Allele Identifier: PA097104
Gene: NPHS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 56448
ClinVar RCV Id: RCV000049861
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004637.1:p.Pro575Gln
CA250138
NM_004646.4:c.1724C>A