Canonical Allele Identifier: PA2827999650
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 485117

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Ser2740Pro
CA16039553
NM_001354901.2:c.8218T>C