Canonical Allele Identifier: PA2829368009
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 3222010
ClinVar RCV Id: RCV004513428

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002221.1:p.Lys12Asn
CA399507264
NM_002230.4:c.36G>T
CA399507266
NM_002230.4:c.36G>C