Canonical Allele Identifier: PA2827981531
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 236656

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Gln2776His
CA10582345
NM_001354899.2:c.8328G>T
CA16039584
NM_001354899.2:c.8328G>C