Canonical Allele Identifier: PA2827680038
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 945673
ClinVar RCV Id: RCV001216371

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339705.1:p.Met76Val
CA399506051
NM_001352776.2:c.226A>G