Canonical Allele Identifier: PA2827959783
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482242

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Ser1768del
CA041117
NM_001354897.2:c.5302_5304del