Canonical Allele Identifier: PA1139741854
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 922223
ClinVar RCV Id: RCV001182155

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Ser2595Pro
CA16038115
NM_001354896.2:c.7783T>C