Canonical Allele Identifier: PA2829368134
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 855054
ClinVar RCV Id: RCV001060226

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002221.1:p.Thr78Ala
CA399506016
NM_002230.4:c.232A>G