Canonical Allele Identifier: PA346573
Gene: NPHS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 180465
ClinVar RCV Id: RCV000157401 RCV002515049 RCV002516361 RCV002498780
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004637.1:p.Gly958Glu
CA346571
NM_004646.4:c.2873G>A