Canonical Allele Identifier: PA353552
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 224553

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Tyr1009Cys
CA353549
NM_001127511.3:c.3026A>G