Canonical Allele Identifier: PA2825018091
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 570044

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Ile1008Val
CA16027942
NM_000038.6:c.3022A>G