Canonical Allele Identifier: PA2828028905
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2452755

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Thr2284Ser
CA16038056
NM_001354906.2:c.6850A>T
CA16038058
NM_001354906.2:c.6851C>G