Canonical Allele Identifier: PA2573205839
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1381000

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Arg2688Gly
CA16038727
NM_001354896.2:c.8062A>G