Canonical Allele Identifier: PA2827972355
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 236656

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Gln2779His
CA10582345
NM_001354898.2:c.8337G>T
CA16039584
NM_001354898.2:c.8337G>C