Canonical Allele Identifier: PA117934
Gene: APOL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 6081

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003652.2:p.Asn388_Tyr389del
CA117932
NM_003661.4:c.1164_1169del