Canonical Allele Identifier: PA2827966447
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 469855

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Met989Val
CA16027984
NM_001354898.2:c.2965A>G