Canonical Allele Identifier: PA2827679455
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 178042

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339704.1:p.Asn309Ser
CA181264
NM_001352775.2:c.926A>G