Canonical Allele Identifier: PA2827678868
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 3064471
ClinVar RCV Id: RCV003989011

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339703.1:p.Gly565Ala
CA399493081
NM_001352774.2:c.1694G>C