Canonical Allele Identifier: PA096767
Gene: NPHS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 180463
ClinVar RCV Id: RCV000157399
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004637.1:p.Arg586Gly
CA346566
NM_004646.4:c.1756A>G