Canonical Allele Identifier: PA645510085
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 438880

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Val1605Met
CA16031876
NM_001127510.3:c.4813G>A