Canonical Allele Identifier: PA2828015989
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 490215

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Arg426Thr
CA16024760
NM_001354903.2:c.1277G>C