Canonical Allele Identifier: PA2827680619
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 323168
ClinVar RCV Id: RCV000303926 RCV000397661
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339705.1:p.Asp573Val
CA10650099
NM_001352776.2:c.1718A>T