Canonical Allele Identifier: PA645402316
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 236650

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Ala2608Thr
CA10582340
NM_001127510.3:c.7822G>A