Canonical Allele Identifier: PA2828046448
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470066

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Thr2163Lys
CA16036318
NM_001354904.2:c.6488C>A