Canonical Allele Identifier: PA2828009669
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482242

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Ser1667del
CA041117
NM_001354902.2:c.4999_5001del