Canonical Allele Identifier: PA2828055629
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2705140
ClinVar RCV Id: RCV003536367

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Thr952Ser
CA16028644
NM_001354905.2:c.2854A>T