Canonical Allele Identifier: PA2828049081
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 851804
ClinVar RCV Id: RCV002240266

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Asn2541Ser
CA16038710
NM_001354904.2:c.7622A>G