Canonical Allele Identifier: PA2827980711
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470102

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Ser2527Leu
CA16037984
NM_001354899.2:c.7580C>T