Canonical Allele Identifier: PA131078
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 21030
ClinVar RCV Id: RCV000020089 RCV000074239 RCV000034393 RCV000035078 RCV000132160 RCV000358689 RCV001270286 RCV002286403 RCV003996112
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Val1822Asp
CA010422
NM_001127510.3:c.5465T>A
CA2838032984
NM_001127510.3:c.5463_5465delinsAGA
CA2850446630
NM_001127510.3:c.5465_5466delinsAT