Canonical Allele Identifier: PA2828008284
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470012

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Pro1683Thr
CA16033423
NM_001354905.2:c.5047C>A