Canonical Allele Identifier: PA2828055302
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181776

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Asn857del
CA008002
NM_001354905.2:c.2569_2571del