Canonical Allele Identifier: PA2828029732
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1381000

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Arg2569Gly
CA16038727
NM_001354903.2:c.7705A>G