Canonical Allele Identifier: PA2827681535
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 191670
ClinVar RCV Id: RCV000171957 RCV000765351 RCV002408745
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339706.1:p.Ile621Thr
CA237205
NM_001352777.2:c.1862T>C