Canonical Allele Identifier: PA658829041
Gene: NPHS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 556151
ClinVar RCV Id: RCV000672110 RCV000821998
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004637.1:p.Asp310Asn
CA9390599
NM_004646.4:c.928G>A