Canonical Allele Identifier: PA916041209
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470066

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Thr2307Lys
CA16036318
NM_001354896.2:c.6920C>A