Canonical Allele Identifier: PA645401796
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411434

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Arg2228Gly
CA16035939
NM_001127510.3:c.6682A>G