Canonical Allele Identifier: PA2827981242
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470132

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Met2685Thr
CA16039005
NM_001354899.2:c.8054T>C