Canonical Allele Identifier: PA2825640242
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411342

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Ile1159Val
CA035626
NM_001127511.3:c.3475A>G