Canonical Allele Identifier: PA1139727204
Gene: NPHS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 990525
ClinVar RCV Id: RCV001278567
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004637.1:p.Arg299His
CA9390604
NM_004646.4:c.896G>A