Canonical Allele Identifier: PA2827971722
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 433677

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Arg2588Lys
CA16038358
NM_001354898.2:c.7763G>A