Canonical Allele Identifier: PA2827681481
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 45839
ClinVar RCV Id: RCV000039068 RCV001241393
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339706.1:p.Ala571Ser
CA137151
NM_001352777.2:c.1711G>T