Canonical Allele Identifier: PA2827985255
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411342

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Ile1136Val
CA035626
NM_001354900.2:c.3406A>G