Canonical Allele Identifier: PA658689362
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 490366

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Phe2620Tyr
CA16038409
NM_001127510.3:c.7859T>A