Canonical Allele Identifier: PA2827961256
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 142044

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Met2223Val
CA012319
NM_001354897.2:c.6667A>G