Canonical Allele Identifier: PA2827946620
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411434

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Arg2228Gly
CA16035939
NM_001354895.2:c.6682A>G