Canonical Allele Identifier: PA916041790
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 133537

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Ala2796Ser
CA014561
NM_001354896.2:c.8386G>T