Canonical Allele Identifier: PA2828004603
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 236656

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Gln2713His
CA10582345
NM_001354902.2:c.8139G>T
CA16039584
NM_001354902.2:c.8139G>C