Canonical Allele Identifier: PA2827677360
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 179756
ClinVar RCV Id: RCV000156554 RCV000253975 RCV000315534 RCV000393399 RCV000656851 RCV000692565 RCV001375636
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339702.1:p.Thr19Ile
CA185075
NM_001352773.2:c.56C>T