Canonical Allele Identifier: PA2827967112
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 141688

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Glu1184Lys
CA008564
NM_001354898.2:c.3550G>A