Canonical Allele Identifier: PA658671953
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 426584

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002221.1:p.Ala458Thr
CA8565223
NM_002230.4:c.1372G>A