Canonical Allele Identifier: PA2827969131
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_001341827.1:p.Val1797Asp
CA010422
NM_001354898.2:c.5390T>A
CA2838032984
NM_001354898.2:c.5388_5390delinsAGA
CA2850446630
NM_001354898.2:c.5390_5391delinsAT