Canonical Allele Identifier: PA658659113
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470152

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Arg302Gln
CA16023293
NM_001127510.3:c.905G>A