Canonical Allele Identifier: PA2827962781
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1320702

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Arg2680Lys
CA16038729
NM_001354897.2:c.8039G>A