Canonical Allele Identifier: PA2827975606
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 469855

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Met986Val
CA16027984
NM_001354899.2:c.2956A>G