Canonical Allele Identifier: PA2827994082
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2705140
ClinVar RCV Id: RCV003536367

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Thr1053Ser
CA16028644
NM_001354901.2:c.3157A>T