Canonical Allele Identifier: PA2828047196
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181817
ClinVar RCV Id: RCV000159569

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Asn2279Ser
CA012942
NM_001354904.2:c.6836A>G