Canonical Allele Identifier: PA2828028682
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181824

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Arg2247Trp
CA013892
NM_001354906.2:c.6739C>T