Canonical Allele Identifier: PA2827680922
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 2942872
ClinVar RCV Id: RCV003808038
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339706.1:p.Met89Lys
CA399505773
NM_001352777.2:c.266T>A