Canonical Allele Identifier: PA2825019106
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 485090

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Ile1164Val
CA16028993
NM_000038.6:c.3490A>G