Canonical Allele Identifier: PA2827681672
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 837932
ClinVar RCV Id: RCV001039374 RCV002427495
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339706.1:p.Gly732Ser
CA8564988
NM_001352777.2:c.2194G>A