Canonical Allele Identifier: PA2827677992
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 1513015
ClinVar RCV Id: RCV002023318
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339702.1:p.Gly553Ala
CA399493322
NM_001352773.2:c.1658G>C