Canonical Allele Identifier: PA2825017988
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411386

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Asp989Gly
CA034127
NM_000038.6:c.2966A>G