Canonical Allele Identifier: PA2828014127
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 236656

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Gln2644His
CA10582345
NM_001354905.2:c.7932G>T
CA16039584
NM_001354905.2:c.7932G>C