Canonical Allele Identifier: PA2827942833
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181799

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Thr1082Ser
CA008176
NM_001354895.2:c.3245C>G
CA16028451
NM_001354895.2:c.3244A>T