Canonical Allele Identifier: PA645417286
Gene: NPHS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 236188
ClinVar RCV Id: RCV000225091
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055440.1:p.Gly35Asp
CA10581522
NM_014625.4:c.104G>A