Canonical Allele Identifier: PA2827998185
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482353

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Ser2293Gly
CA16036702
NM_001354901.2:c.6877A>G