Canonical Allele Identifier: PA2825024766
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1760336
ClinVar RCV Id: RCV002400712

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Ser2577Thr
CA16038114
NM_000038.6:c.7729T>A