Canonical Allele Identifier: PA2827680609
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 201827

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339705.1:p.Ile569Phe
CA308546
NM_001352776.2:c.1705A>T