Canonical Allele Identifier: PA096670
Gene: NPHS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 56473
ClinVar RCV Id: RCV000049886 RCV000712426
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004637.1:p.Ala806Asp
CA250185
NM_004646.4:c.2417C>A