Canonical Allele Identifier: PA2827954033
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2624856

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Tyr1049Cys
CA16028105
NM_001354896.2:c.3146A>G