Canonical Allele Identifier: PA645398906
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 231917

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Thr518Met
CA028394
NM_001127510.3:c.1553C>T