Canonical Allele Identifier: PA237244
Gene: JUP HGNC NCBI

Linked Data

ClinVar Variation Id: 191677
ClinVar RCV Id: RCV000171965 RCV001067921
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_068831.1:p.Asn112Ser
CA237240
NM_021991.4:c.335A>G