Canonical Allele Identifier: PA2827998864
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1447119
ClinVar RCV Id: RCV002563486

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Ser2498Thr
CA16037990
NM_001354901.2:c.7492T>A