Canonical Allele Identifier: PA2828029757
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2677396

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Ser2573Pro
CA16038751
NM_001354903.2:c.7717T>C