Canonical Allele Identifier: PA2827679038
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 201805
ClinVar RCV Id: RCV000183478 RCV000767068 RCV001327335 RCV002415781
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339703.1:p.Asp708Asn
CA308431
NM_001352774.2:c.2122G>A