Canonical Allele Identifier: PA2827679976
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 1422349
ClinVar RCV Id: RCV001919493
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339705.1:p.Ser28Leu
CA290701403
NM_001352776.2:c.83C>T