Canonical Allele Identifier: PA2828036419
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 469855

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Met888Val
CA16027984
NM_001354904.2:c.2662A>G