Canonical Allele Identifier: PA2573071465
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1318535

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Ala2748Asp
CA16039108
NM_001354896.2:c.8243C>A