Canonical Allele Identifier: PA2827678946
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 180377
ClinVar RCV Id: RCV000157252 RCV002408706 RCV002492607
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339703.1:p.Ala628Thr
CA346371
NM_001352774.2:c.1882G>A