Canonical Allele Identifier: PA2827939680
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 420793

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Arg88Trp
CA032840
NM_001354895.2:c.262C>T