Canonical Allele Identifier: PA2827677713
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 201819
ClinVar RCV Id: RCV000251525 RCV000475317 RCV000587522 RCV001293416
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339702.1:p.Gly298Ser
CA308501
NM_001352773.2:c.892G>A