Canonical Allele Identifier: PA2829369092
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 519077

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002221.1:p.Arg582Gln
CA290695975
NM_002230.4:c.1745G>A