Canonical Allele Identifier: PA2828041768
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 231898

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Met1512Thr
CA040178
NM_001354904.2:c.4535T>C