Canonical Allele Identifier: PA2828007818
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482242

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Ser1598del
CA041117
NM_001354905.2:c.4792_4794del