Canonical Allele Identifier: PA2827972069
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470132

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Met2688Thr
CA16039005
NM_001354898.2:c.8063T>C