Canonical Allele Identifier: PA2580307122
Gene: NPHS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1712391

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004637.1:p.Lys848Thr
CA9390089
NM_004646.4:c.2543A>C