Canonical Allele Identifier: PA1139736287
Gene: NPHS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 974486
ClinVar RCV Id: RCV001281253
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055440.1:p.Ala318del
CA891813344
NM_014625.4:c.953_955del