Canonical Allele Identifier: PA191263
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 185188

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Ala61Thr
CA006037
NM_000038.6:c.181G>A