Canonical Allele Identifier: PA2828049082
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1761613

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Asn2542del
CA2580072453
NM_001354904.2:c.7623_7625del