Canonical Allele Identifier: PA2825024691
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1447119
ClinVar RCV Id: RCV002563486

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Ser2557Thr
CA16037990
NM_000038.6:c.7669T>A