Canonical Allele Identifier: PA2827999235
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1320702

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Arg2611Lys
CA16038729
NM_001354901.2:c.7832G>A