Canonical Allele Identifier: PA2827971573
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1760169
ClinVar RCV Id: RCV002400545

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Arg2541Ile
CA16038051
NM_001354898.2:c.7622G>T