Canonical Allele Identifier: PA237243
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 191677
ClinVar RCV Id: RCV000171965 RCV001067921
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002221.1:p.Asn112Ser
CA237240
NM_002230.4:c.335A>G