Canonical Allele Identifier: PA2828019061
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 822912
ClinVar RCV Id: RCV001018680
ClinVar Variation Id: 2452689
ClinVar RCV Id: RCV003177463

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Asn754Lys
CA16028150
NM_001354906.2:c.2262C>A
CA16028151
NM_001354906.2:c.2262C>G