Canonical Allele Identifier: PA2828030006
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1318535

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Ala2447Asp
CA16039108
NM_001354906.2:c.7340C>A