Canonical Allele Identifier: PA2827977817
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411414

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Arg1648del
CA3368170
NM_001354899.2:c.4942_4944del