Canonical Allele Identifier: PA658831747
Gene: NPHS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 556375
ClinVar RCV Id: RCV000672374 RCV001662741
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055440.1:p.Leu327Phe
CA1267046
NM_014625.4:c.979C>T