Canonical Allele Identifier: PA2827678809
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 1405334
ClinVar RCV Id: RCV001903725

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339703.1:p.His515Arg
CA399493998
NM_001352774.2:c.1544A>G