Canonical Allele Identifier: PA2827681629
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 21304

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339706.1:p.Met697Leu
CA137178
NM_001352777.2:c.2089A>T
CA399490809
NM_001352777.2:c.2089A>C