Canonical Allele Identifier: PA1139741891
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 941683

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Pro2640Gln
CA1139659004
NM_001354896.2:c.7919_7920delinsAG