Canonical Allele Identifier: PA2499252370
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1039177

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Thr2616Ser
CA16038256
NM_001354896.2:c.7846A>T
CA16038257
NM_001354896.2:c.7847C>G