Canonical Allele Identifier: PA2827953212
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1759132

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Ser2515Thr
CA16037620
NM_001354896.2:c.7543T>A