Canonical Allele Identifier: PA2827971748
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 941683

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Pro2597Gln
CA1139659004
NM_001354898.2:c.7790_7791delinsAG