Canonical Allele Identifier: PA2827678578
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 855662

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339703.1:p.Leu295Pro
CA399500634
NM_001352774.2:c.884T>C