Canonical Allele Identifier: PA2827967420
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 186133

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Ile1279Val
CA008754
NM_001354898.2:c.3835A>G