Canonical Allele Identifier: PA2827971920
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1320702

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Arg2645Lys
CA16038729
NM_001354898.2:c.7934G>A