Canonical Allele Identifier: PA2827677434
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 1417055
ClinVar RCV Id: RCV001923502 RCV004043556
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339702.1:p.Met76Ile
CA8565544
NM_001352773.2:c.228G>A
CA399506036
NM_001352773.2:c.228G>T
CA399506038
NM_001352773.2:c.228G>C