Canonical Allele Identifier: PA2827681311
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 536630
ClinVar RCV Id: RCV000645205 RCV002449040
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339706.1:p.Asn421Ser
CA8565243
NM_001352777.2:c.1262A>G