Canonical Allele Identifier: PA16039870
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 236567

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Ile676Val
CA030596
NM_000038.6:c.2026A>G