Canonical Allele Identifier: PA2828014528
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
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Ser23Arg
CA015653
NM_001354906.2:c.69T>G
CA16023314
NM_001354906.2:c.67A>C
CA16023320
NM_001354906.2:c.69T>A