Canonical Allele Identifier: PA645375300
Gene: NPHS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 290122
ClinVar RCV Id: RCV000361967 RCV001125721 RCV001272299 RCV003417918
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004637.1:p.Ser220Ala
CA9390706
NM_004646.4:c.658T>G