Canonical Allele Identifier: PA2828029150
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 933245
ClinVar RCV Id: RCV003538603

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Ser2318Thr
CA16038278
NM_001354906.2:c.6953G>C