Canonical Allele Identifier: PA2827680617
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 45840

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339705.1:p.Arg572Leu
CA137156
NM_001352776.2:c.1715G>T