Canonical Allele Identifier: PA2827992864
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 566805

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Lys679Arg
CA16026181
NM_001354901.2:c.2036A>G