Canonical Allele Identifier: PA2827681549
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 180377
ClinVar RCV Id: RCV000157252 RCV002408706 RCV002492607
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339706.1:p.Ala628Thr
CA346371
NM_001352777.2:c.1882G>A