Canonical Allele Identifier: PA2827680804
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 837932

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339705.1:p.Gly732Ser
CA8564988
NM_001352776.2:c.2194G>A