Canonical Allele Identifier: PA2828034311
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 185391

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Val578Ile
CA007204
NM_001354904.2:c.1732G>A