Canonical Allele Identifier: PA2827678203
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 1439390
ClinVar RCV Id: RCV001974948 RCV002425294
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339702.1:p.Pro735Leu
CA8564987
NM_001352773.2:c.2204C>T