Canonical Allele Identifier: PA2825013715
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470104

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Asp256Glu
CA16023011
NM_000038.6:c.768T>A
CA16023012
NM_000038.6:c.768T>G