Canonical Allele Identifier: PA2828017757
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 485094

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Arg562Cys
CA16026883
NM_001354906.2:c.1684C>T