Canonical Allele Identifier: PA2827680809
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 45847

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339705.1:p.Pro736Leu
CA137193
NM_001352776.2:c.2207C>T