Canonical Allele Identifier: PA2827965992
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482506

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Gly852Ala
CA032861
NM_001354898.2:c.2555G>C