Canonical Allele Identifier: PA2827968920
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482242

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Ser1733del
CA041117
NM_001354898.2:c.5197_5199del