Canonical Allele Identifier: PA2827979976
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 628104
ClinVar RCV Id: RCV000772409

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Ser2302Thr
CA16036564
NM_001354899.2:c.6904T>A