Canonical Allele Identifier: PA2828019029
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2624856

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Tyr748Cys
CA16028105
NM_001354906.2:c.2243A>G