Canonical Allele Identifier: PA2827949581
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181783
ClinVar RCV Id: RCV000159528 RCV000217691 RCV000466236 RCV000779736 RCV003650405 RCV003998401
ClinVar Variation Id: 919990
ClinVar RCV Id: RCV001178470
ClinVar Variation Id: 3231860
ClinVar RCV Id: RCV004518575
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Ser306Arg
CA015653
NM_001354896.2:c.918T>G
CA16023314
NM_001354896.2:c.916A>C
CA16023320
NM_001354896.2:c.918T>A