Canonical Allele Identifier: PA2829369321
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 958935

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002221.1:p.Ser730Asn
CA8564991
NM_002230.4:c.2189G>A