Canonical Allele Identifier: PA2580446220
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_068831.1:p.Met704Val
CA399490736
NM_021991.4:c.2110A>G