Canonical Allele Identifier: PA2827680868
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 660738
ClinVar RCV Id: RCV000817995
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339706.1:p.Asp46Asn
CA8565577
NM_001352777.2:c.136G>A