Canonical Allele Identifier: PA096888
Gene: NPHS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 56443
ClinVar RCV Id: RCV000049856
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004637.1:p.Cys528Phe
CA250127
NM_004646.4:c.1583G>T