Canonical Allele Identifier: PA916042630
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411342

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Ile894Val
CA035626
NM_001354906.2:c.2680A>G