Canonical Allele Identifier: PA2827681465
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 239104
ClinVar RCV Id: RCV000231900 RCV000439893 RCV000617763
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339706.1:p.Met556Thr
CA8565152
NM_001352777.2:c.1667T>C