Canonical Allele Identifier: PA2829369341
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 1016429

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002221.1:p.Met743Val
CA399490218
NM_002230.4:c.2227A>G