Canonical Allele Identifier: PA2828012756
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1760236
ClinVar RCV Id: RCV002400612

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Ser2409Thr
CA16038070
NM_001354905.2:c.7226G>C