Canonical Allele Identifier: PA2827955251
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1368868

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Thr307Ile
CA16023266
NM_001354897.2:c.920C>T