Canonical Allele Identifier: PA2828029086
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 628605
ClinVar RCV Id: RCV000773146

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.His2308Tyr
CA16038214
NM_001354906.2:c.6922C>T