Canonical Allele Identifier: PA2825635367
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1320702

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Arg2670Lys
CA16038729
NM_001127510.3:c.8009G>A