Canonical Allele Identifier: PA2827679910
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 468749
ClinVar RCV Id: RCV000535229 RCV001764577
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339704.1:p.Pro710Ser
CA8565002
NM_001352775.2:c.2128C>T