Canonical Allele Identifier: PA2828023007
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 231898

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Met1537Thr
CA040178
NM_001354903.2:c.4610T>C