Canonical Allele Identifier: PA2825015764
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 469719

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Val588Ile
CA029508
NM_000038.6:c.1762G>A