Canonical Allele Identifier: PA2829777809
Gene: NPHP4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1431959
ClinVar RCV Id: RCV001941020

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055917.1:p.Ala1333Gly
CA338049325
NM_015102.5:c.3998C>G