Canonical Allele Identifier: PA2829368149
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 863405
ClinVar RCV Id: RCV001070361

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002221.1:p.Ala88Asn
CA916081885
NM_002230.4:c.262_263delinsAA