Canonical Allele Identifier: PA2827971908
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1761613

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Asn2643del
CA2580072453
NM_001354898.2:c.7926_7928del