Canonical Allele Identifier: PA2825024924
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 490366

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Phe2620Tyr
CA16038409
NM_000038.6:c.7859T>A