Canonical Allele Identifier: PA137159
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 45840

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002221.1:p.Arg572Leu
CA137156
NM_002230.4:c.1715G>T