Canonical Allele Identifier: PA2827975321
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181768

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Ala900Thr
CA007787
NM_001354899.2:c.2698G>A