Canonical Allele Identifier: PA096958
Gene: NPHS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 56508
ClinVar RCV Id: RCV000049921
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004637.1:p.Ile171Asn
CA250245
NM_004646.4:c.512T>A