Canonical Allele Identifier: PA2827980914
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 490366

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Phe2592Tyr
CA16038409
NM_001354899.2:c.7775T>A