Canonical Allele Identifier: PA2828049436
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1318535

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Ala2604Asp
CA16039108
NM_001354904.2:c.7811C>A