Canonical Allele Identifier: PA2827679035
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 1897535
ClinVar RCV Id: RCV002572430
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339703.1:p.Met704Val
CA399490736
NM_001352774.2:c.2110A>G