Canonical Allele Identifier: PA2827971933
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2677396

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Ser2649Pro
CA16038751
NM_001354898.2:c.7945T>C