Canonical Allele Identifier: PA2828053942
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 428132

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Arg480Trp
CA16025509
NM_001354905.2:c.1438C>T