Canonical Allele Identifier: PA2825018231
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2624856

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Tyr1031Cys
CA16028105
NM_000038.6:c.3092A>G