Canonical Allele Identifier: PA2827679267
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 468754

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339704.1:p.Val159Leu
CA8565461
NM_001352775.2:c.475G>T
CA399503654
NM_001352775.2:c.475G>C