Canonical Allele Identifier: PA2828032014
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411556

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Arg234Trp
CA049073
NM_001354904.2:c.700C>T