Canonical Allele Identifier: PA16040141
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 236650

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Ala2608Thr
CA10582340
NM_000038.6:c.7822G>A