ClinGen Allele Registry
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Canonical Allele Identifier:
PA144292
Gene: CUBN
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000049751
ClinVar Variation:
56338
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001072.2:p.Thr1372Arg
CA144290
NM_001081.4:c.4115C>G