Canonical Allele Identifier: PA181268
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 178042
ClinVar RCV Id: RCV000154727 RCV000171961 RCV000467285 RCV002372009
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_068831.1:p.Asn309Ser
CA181264
NM_021991.4:c.926A>G