Canonical Allele Identifier: PA346562
Gene: NPHS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 180460

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004637.1:p.Leu433Phe
CA346560
NM_004646.4:c.1297C>T