Canonical Allele Identifier: PA2825022309
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1171348

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Thr1947Ile
CA16034105
NM_000038.6:c.5840C>T