Canonical Allele Identifier: PA2580307036
Gene: NPHS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2253646
ClinVar RCV Id: RCV002758110

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004637.1:p.His320Gln
CA307787638
NM_004646.4:c.960C>A
CA405406726
NM_004646.4:c.960C>G