Canonical Allele Identifier: PA2827974200
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 156480

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Thr534Met
CA005437
NM_001354899.2:c.1601C>T