Canonical Allele Identifier: PA2827678943
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 201829

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339703.1:p.Ser627Leu
CA308556
NM_001352774.2:c.1880C>T