Canonical Allele Identifier: PA2825017511
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 428176

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Leu922Phe
CA033363
NM_000038.6:c.2764C>T