Canonical Allele Identifier: PA2827681186
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 222662
ClinVar RCV Id: RCV000208313 RCV000213286 RCV000996539 RCV000798524
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339706.1:p.Glu301Gly
CA353980
NM_001352777.2:c.902A>G