Canonical Allele Identifier: PA137181
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 21304

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002221.1:p.Met697Leu
CA137178
NM_002230.4:c.2089A>T
CA399490809
NM_002230.4:c.2089A>C