Canonical Allele Identifier: PA2827680040
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 3222009
ClinVar RCV Id: RCV004513427

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339705.1:p.Ser77Pro
CA399506034
NM_001352776.2:c.229T>C