Canonical Allele Identifier: PA658671835
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 468754

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_068831.1:p.Val159Leu
CA8565461
NM_021991.4:c.475G>T
CA399503654
NM_021991.4:c.475G>C