Canonical Allele Identifier: PA2827680823
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 966967
ClinVar RCV Id: RCV001241769
ClinVar Variation Id: 1468273
ClinVar RCV Id: RCV001993615 RCV002074445
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339706.1:p.Met7Ile
CA8565602
NM_001352777.2:c.21G>C
CA399507332
NM_001352777.2:c.21G>T
CA399507335
NM_001352777.2:c.21G>A