Canonical Allele Identifier: PA2573240059
Gene: NPHS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1401486
ClinVar RCV Id: RCV001906313

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004637.1:p.Ile397Leu
CA405405855
NM_004646.4:c.1189A>C