Canonical Allele Identifier: PA2828019087
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2624856

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Tyr930Cys
CA16028105
NM_001354903.2:c.2789A>G