Canonical Allele Identifier: PA2827677957
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 1492213
ClinVar RCV Id: RCV001980782

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339702.1:p.Arg526Ser
CA399493817
NM_001352773.2:c.1576C>A