ClinGen Allele Registry
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Canonical Allele Identifier:
PA2827681668
Gene: JUP
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV001232198
RCV001760237
RCV002429990
ClinVar Variation:
958935
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001339706.1:p.Ser730Asn
CA8564991
NM_001352777.2:c.2189G>A