Canonical Allele Identifier: PA2827953436
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1761613

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Asn2686del
CA2580072453
NM_001354896.2:c.8055_8057del