Canonical Allele Identifier: PA2828037651
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411342

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Ile1051Val
CA035626
NM_001354904.2:c.3151A>G