Canonical Allele Identifier: PA2828014883
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411556

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Arg259Trp
CA049073
NM_001354903.2:c.775C>T