Canonical Allele Identifier: PA2573280547
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 1450398

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_068831.1:p.Ala162Ser
CA399503612
NM_021991.4:c.484G>T