Canonical Allele Identifier: PA2828029047
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 230982

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Lys2302Thr
CA10578450
NM_001354906.2:c.6905A>C